ENST00000254108.12:c.571G=
MANE Select
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ENSP00000254108.8:p.Gly191=
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ENST00000254108.11:c.571G=
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ENSP00000254108.7:p.Gly191=
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ENST00000380244.7:c.568G=
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ENSP00000369594.3:p.Gly190=
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ENST00000487509.6:n.636G=
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|
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ENST00000566605.5:c.571G=
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ENSP00000455073.1:p.Gly191=
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ENST00000568685.1:c.571G=
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ENSP00000455282.1:p.Gly191=
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NM_001170634.1:c.568G=
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NP_001164105.1:p.Gly190=
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NM_001170937.1:c.559G=
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NP_001164408.1:p.Gly187=
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NM_004960.3:c.571G= , LRG_655t1:c.571G=
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NP_004951.1:p.Gly191=
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NR_028388.2:n.676G=
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|
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XM_005255233.3:c.-10G=
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XP_005255290.1:n.-10G=
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|
XM_011545781.1:c.565G=
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XP_011544083.1:p.Gly189=
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XM_011545782.1:c.-10G=
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XP_011544084.1:n.-10G=
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XM_005255233.5:c.-10G=
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XP_005255290.1:n.-10G=
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XM_011545782.2:c.-10G=
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XP_011544084.1:n.-10G=
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XM_024450221.1:c.562G=
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XP_024305989.1:p.Gly188=
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NM_004960.4:c.571G=
MANE Select
|
NP_004951.1:p.Gly191=
|
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