ENST00000281928.9:c.3377G>C
MANE Select
|
ENSP00000281928.3:p.Arg1126Thr
|
|
ENST00000549786.2:c.2805G>C
|
|
|
ENST00000648379.1:n.1745G>C
|
|
|
ENST00000648737.1:n.3141G>C
|
|
|
ENST00000648825.1:n.117G>C
|
|
|
ENST00000648916.1:n.1388G>C
|
|
|
ENST00000649607.1:c.1561G>C
|
|
|
ENST00000650226.1:c.3377G>C
|
ENSP00000496981.1:p.Arg1126Thr
|
|
ENST00000281928.7:c.3377G>C
|
ENSP00000281928.3:p.Arg1126Thr
|
|
NM_015335.4:c.3377G>C
|
NP_056150.1:p.Arg1126Thr
|
|
XM_011538080.1:c.3377G>C
|
XP_011536382.1:p.Arg1126Thr
|
|
XM_011538081.1:c.3374G>C
|
XP_011536383.1:p.Arg1125Thr
|
|
XM_011538082.1:c.3347G>C
|
XP_011536384.1:p.Arg1116Thr
|
|
XM_011538080.2:c.3377G>C
|
XP_011536382.1:p.Arg1126Thr
|
|
XM_011538081.2:c.3374G>C
|
XP_011536383.1:p.Arg1125Thr
|
|
XM_011538082.2:c.3347G>C
|
XP_011536384.1:p.Arg1116Thr
|
|
XM_017019090.1:c.3374G>C
|
XP_016874579.1:p.Arg1125Thr
|
|
NM_015335.5:c.3377G>C
MANE Select
|
NP_056150.1:p.Arg1126Thr
|
|