ENST00000375731.9:c.658G>T
MANE Select
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ENSP00000364883.5:p.Gly220Trp
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ENST00000303617.5:c.571G>T
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ENSP00000307334.5:p.Gly191Trp
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ENST00000375731.8:c.658G>T
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ENSP00000364883.4:p.Gly220Trp
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NM_001306190.1:c.571G>T
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NP_001293119.1:p.Gly191Trp
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NM_001698.2:c.658G>T , LRG_449t1:c.658G>T
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NP_001689.1:p.Gly220Trp
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XM_005252066.2:c.688G>T
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XP_005252123.1:p.Gly230Trp
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XM_005252067.3:c.688G>T
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XP_005252124.1:p.Gly230Trp
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XM_005252069.3:c.688G>T
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XP_005252126.1:p.Gly230Trp
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XM_005252073.2:c.196G>T
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XP_005252130.1:p.Gly66Trp
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XM_006717150.2:c.601G>T
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XP_006717213.1:p.Gly201Trp
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XM_011518801.1:c.334G>T
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XP_011517103.1:p.Gly112Trp
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XM_011518802.1:c.331G>T
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XP_011517104.1:p.Gly111Trp
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NM_001351431.1:c.331G>T
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NP_001338360.1:p.Gly111Trp
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NM_001351432.1:c.331G>T
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NP_001338361.1:p.Gly111Trp
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NM_001351433.1:c.331G>T
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NP_001338362.1:p.Gly111Trp
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XM_005252066.3:c.688G>T
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XP_005252123.1:p.Gly230Trp
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XM_005252067.4:c.688G>T
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XP_005252124.1:p.Gly230Trp
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XM_005252069.4:c.688G>T
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XP_005252126.1:p.Gly230Trp
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XM_006717150.3:c.601G>T
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XP_006717213.1:p.Gly201Trp
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XM_017014849.1:c.658G>T
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XP_016870338.1:p.Gly220Trp
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XR_001746328.2:n.883G>T
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XR_001746329.2:n.835G>T
|
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NM_001698.3:c.658G>T
MANE Select
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NP_001689.1:p.Gly220Trp
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NM_001306190.2:c.571G>T
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NP_001293119.1:p.Gly191Trp
|
|
NM_001351431.2:c.331G>T
|
NP_001338360.1:p.Gly111Trp
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|
NM_001351432.2:c.331G>T
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NP_001338361.1:p.Gly111Trp
|
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NM_001351433.2:c.331G>T
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NP_001338362.1:p.Gly111Trp
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