ENST00000315757.9:c.1278G>C
MANE Select
|
ENSP00000327290.7:p.Gly426=
|
|
ENST00000315757.8:c.1278G>C
|
ENSP00000327290.7:p.Gly426=
|
|
ENST00000423218.6:c.1278G>C
|
ENSP00000403392.2:p.Gly426=
|
|
ENST00000566429.1:n.197-30G>C
|
|
|
ENST00000569346.5:n.257G>C
|
|
|
NM_001004439.1:c.1278G>C
|
NP_001004439.1:p.Gly426=
|
|
XM_005254228.2:c.972G>C
|
XP_005254285.1:p.Gly324=
|
|
XM_011521363.1:c.1071G>C
|
XP_011519665.1:p.Gly357=
|
|
XM_005254228.3:c.972G>C
|
XP_005254285.1:p.Gly324=
|
|
XM_011521363.2:c.1071G>C
|
XP_011519665.1:p.Gly357=
|
|
NM_001004439.2:c.1278G>C
MANE Select
|
NP_001004439.1:p.Gly426=
|
|