ENST00000256646.7:c.1312G>A
MANE Select
|
ENSP00000256646.2:p.Gly438Ser
|
|
ENST00000640021.1:c.532G>A
|
ENSP00000492223.1:n.532G>A
|
|
ENST00000256646.6:c.1312G>A
|
ENSP00000256646.2:p.Gly438Ser
|
|
ENST00000479412.2:n.1450G>A
|
|
|
ENST00000579475.7:c.1195G>A
|
ENSP00000477065.2:p.Gly399Ser
|
|
NM_001200001.1:c.1312G>A
|
NP_001186930.1:p.Gly438Ser
|
|
NM_024408.3:c.1312G>A
|
NP_077719.2:p.Gly438Ser
|
|
XM_005270901.2:c.1195G>A
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XP_005270958.1:p.Gly399Ser
|
|
XM_011541519.1:c.1300G>A
|
XP_011539821.1:p.Gly434Ser
|
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XM_011541520.1:c.1195G>A
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XP_011539822.1:p.Gly399Ser
|
|
NM_024408.4:c.1312G>A
MANE Select
|
NP_077719.2:p.Gly438Ser
|
|
NM_001200001.2:c.1312G>A
|
NP_001186930.1:p.Gly438Ser
|
|