ENST00000299084.9:c.890G>T
MANE Select
|
ENSP00000299084.4:p.Gly297Val
|
|
ENST00000299084.8:c.890G>T
|
ENSP00000299084.4:p.Gly297Val
|
|
NM_152594.2:c.890G>T
|
NP_689807.1:p.Gly297Val
|
|
XM_005254202.2:c.926G>T
|
XP_005254259.1:p.Gly309Val
|
|
XM_005254203.3:c.668G>T
|
XP_005254260.1:p.Gly223Val
|
|
XM_011521288.1:c.827G>T
|
XP_011519590.1:p.Gly276Val
|
|
XM_011521289.1:c.827G>T
|
XP_011519591.1:p.Gly276Val
|
|
XM_011521290.1:c.827G>T
|
XP_011519592.1:p.Gly276Val
|
|
XM_005254202.3:c.926G>T
|
XP_005254259.1:p.Gly309Val
|
|
XM_011521289.3:c.827G>T
|
XP_011519591.1:p.Gly276Val
|
|
NM_152594.3:c.890G>T
MANE Select
|
NP_689807.1:p.Gly297Val
|
|