ENST00000367268.5:c.1069G>T
MANE Select
|
ENSP00000356237.4:p.Val357Phe
|
|
ENST00000367267.5:c.1069G>T
|
ENSP00000356236.1:p.Val357Phe
|
|
ENST00000367268.4:c.1069G>T
|
ENSP00000356237.4:p.Val357Phe
|
|
NM_001136504.1:c.1069G>T
|
NP_001129976.1:p.Val357Phe
|
|
NM_177402.4:c.1069G>T
|
NP_796376.2:p.Val357Phe
|
|
XM_011509192.1:c.1078G>T
|
XP_011507494.1:p.Val360Phe
|
|
XM_011509192.2:c.1078G>T
|
XP_011507494.1:p.Val360Phe
|
|
XM_017000309.2:c.1249G>T
|
XP_016855798.1:p.Val417Phe
|
|
XM_017000310.2:c.1240G>T
|
XP_016855799.1:p.Val414Phe
|
|
XM_017000311.2:c.1078G>T
|
XP_016855800.1:p.Val360Phe
|
|
XM_017000312.1:c.1078G>T
|
XP_016855801.1:p.Val360Phe
|
|
XM_017000313.1:c.1069G>T
|
XP_016855802.1:p.Val357Phe
|
|
NM_177402.5:c.1069G>T
MANE Select
|
NP_796376.2:p.Val357Phe
|
|