ENST00000420175.3:c.380G>T
MANE Select
|
ENSP00000391137.2:p.Gly127Val
|
|
ENST00000275838.5:c.380G>T
|
ENSP00000275838.1:p.Gly127Val
|
|
ENST00000377867.7:c.335G>T
|
ENSP00000367098.3:p.Gly112Val
|
|
ENST00000420175.2:c.380G>T
|
ENSP00000391137.2:p.Gly127Val
|
|
NM_001142459.1:c.380G>T
|
NP_001135931.2:p.Gly127Val
|
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NM_001142460.1:c.380G>T
|
NP_001135932.2:p.Gly127Val
|
|
NM_080871.3:c.335G>T
|
NP_543147.2:p.Gly112Val
|
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XM_005249949.3:c.515G>T
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XP_005250006.1:p.Gly172Val
|
|
NM_001142459.2:c.380G>T
MANE Select
|
NP_001135931.2:p.Gly127Val
|
|
NM_080871.4:c.335G>T
|
NP_543147.2:p.Gly112Val
|
|