ENST00000367268.5:c.1232T>A
MANE Select
|
ENSP00000356237.4:p.Val411Glu
|
|
ENST00000367267.5:c.1232T>A
|
ENSP00000356236.1:p.Val411Glu
|
|
ENST00000367268.4:c.1232T>A
|
ENSP00000356237.4:p.Val411Glu
|
|
NM_001136504.1:c.1232T>A
|
NP_001129976.1:p.Val411Glu
|
|
NM_177402.4:c.1232T>A
|
NP_796376.2:p.Val411Glu
|
|
XM_011509192.1:c.1241T>A
|
XP_011507494.1:p.Val414Glu
|
|
XM_011509192.2:c.1241T>A
|
XP_011507494.1:p.Val414Glu
|
|
XM_017000309.2:c.1412T>A
|
XP_016855798.1:p.Val471Glu
|
|
XM_017000310.2:c.1403T>A
|
XP_016855799.1:p.Val468Glu
|
|
XM_017000311.2:c.1241T>A
|
XP_016855800.1:p.Val414Glu
|
|
XM_017000312.1:c.1241T>A
|
XP_016855801.1:p.Val414Glu
|
|
XM_017000313.1:c.1232T>A
|
XP_016855802.1:p.Val411Glu
|
|
NM_177402.5:c.1232T>A
MANE Select
|
NP_796376.2:p.Val411Glu
|
|