ENST00000254108.12:c.536A=
MANE Select
|
ENSP00000254108.8:p.Gln179=
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|
ENST00000254108.11:c.536A=
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ENSP00000254108.7:p.Gln179=
|
|
ENST00000380244.7:c.533A=
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ENSP00000369594.3:p.Gln178=
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|
ENST00000487509.6:n.601A=
|
|
|
ENST00000566605.5:c.536A=
|
ENSP00000455073.1:p.Gln179=
|
|
ENST00000568685.1:c.536A=
|
ENSP00000455282.1:p.Gln179=
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|
NM_001170634.1:c.533A=
|
NP_001164105.1:p.Gln178=
|
|
NM_001170937.1:c.524A=
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NP_001164408.1:p.Gln175=
|
|
NM_004960.3:c.536A= , LRG_655t1:c.536A=
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NP_004951.1:p.Gln179=
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|
NR_028388.2:n.641A=
|
|
|
XM_005255233.3:c.-45A=
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XP_005255290.1:n.-45A=
|
|
XM_011545781.1:c.530A=
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XP_011544083.1:p.Gln177=
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|
XM_011545782.1:c.-45A=
|
XP_011544084.1:n.-45A=
|
|
XM_005255233.5:c.-45A=
|
XP_005255290.1:n.-45A=
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|
XM_011545782.2:c.-45A=
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XP_011544084.1:n.-45A=
|
|
XM_024450221.1:c.527A=
|
XP_024305989.1:p.Gln176=
|
|
NM_004960.4:c.536A=
MANE Select
|
NP_004951.1:p.Gln179=
|
|