ENST00000299084.9:c.1331G>T
MANE Select
|
ENSP00000299084.4:p.Gly444Val
|
|
ENST00000299084.8:c.1331G>T
|
ENSP00000299084.4:p.Gly444Val
|
|
NM_152594.2:c.1331G>T
|
NP_689807.1:p.Gly444Val
|
|
XM_005254202.2:c.1367G>T
|
XP_005254259.1:p.Gly456Val
|
|
XM_005254203.3:c.1109G>T
|
XP_005254260.1:p.Gly370Val
|
|
XM_011521288.1:c.1268G>T
|
XP_011519590.1:p.Gly423Val
|
|
XM_011521289.1:c.1268G>T
|
XP_011519591.1:p.Gly423Val
|
|
XM_011521290.1:c.1268G>T
|
XP_011519592.1:p.Gly423Val
|
|
XM_005254202.3:c.1367G>T
|
XP_005254259.1:p.Gly456Val
|
|
XM_011521289.3:c.1268G>T
|
XP_011519591.1:p.Gly423Val
|
|
NM_152594.3:c.1331G>T
MANE Select
|
NP_689807.1:p.Gly444Val
|
|