ENST00000624552.4:c.14878G>A
|
ENSP00000485357.2:p.Gly4960Ser
|
|
ENST00000683500.2:c.14935G>A
MANE Select
|
ENSP00000508292.2:p.Gly4979Ser
|
|
ENST00000623487.1:n.3281G>A
|
|
|
ENST00000624552.3:c.14875G>A
|
ENSP00000485357.1:p.Gly4959Ser
|
|
NM_001291815.1:c.14935G>A
|
NP_001278744.1:p.Gly4979Ser
|
|
XM_011518465.1:c.14812G>A
|
XP_011516767.1:p.Gly4938Ser
|
|
XM_011518466.1:c.14803G>A
|
XP_011516768.1:p.Gly4935Ser
|
|
XM_011518467.1:c.14758G>A
|
XP_011516769.1:p.Gly4920Ser
|
|
NM_001291815.2:c.14935G>A
MANE Select
|
NP_001278744.1:p.Gly4979Ser
|
|
XM_011518465.2:c.14812G>A
|
XP_011516767.1:p.Gly4938Ser
|
|
XM_011518466.2:c.14803G>A
|
XP_011516768.1:p.Gly4935Ser
|
|
XM_011518467.2:c.14758G>A
|
XP_011516769.1:p.Gly4920Ser
|
|
XM_017014585.1:c.11716G>A
|
XP_016870074.1:p.Gly3906Ser
|
|
XM_017014586.1:c.7513G>A
|
XP_016870075.1:p.Gly2505Ser
|
|
XR_001746957.1:n.92+233C>T
|
|
|
XR_001746958.1:n.92+233C>T
|
|
|