ENST00000334554.12:c.385G>T
MANE Select
|
ENSP00000334490.7:p.Asp129Tyr
|
|
ENST00000320602.11:c.384+85G>T
|
ENSP00000317804.7:n.384+85G>T
|
|
ENST00000334554.11:c.385G>T
|
ENSP00000334490.7:p.Asp129Tyr
|
|
ENST00000405930.3:c.385G>T
|
ENSP00000384716.3:p.Asp129Tyr
|
|
ENST00000436518.5:c.352G>T
|
ENSP00000412807.1:p.Asp118Tyr
|
|
ENST00000468112.5:n.58-897G>T
|
|
|
NM_001185024.1:c.385G>T
|
NP_001171953.1:p.Asp129Tyr
|
|
NM_013373.3:c.385G>T
|
NP_037505.1:p.Asp129Tyr
|
|
XM_006724239.2:c.385G>T
|
XP_006724302.1:p.Asp129Tyr
|
|
NM_001185024.2:c.385G>T
|
NP_001171953.1:p.Asp129Tyr
|
|
NM_013373.4:c.385G>T
MANE Select
|
NP_037505.1:p.Asp129Tyr
|
|