ENST00000378750.10:c.953G>C
MANE Select
|
ENSP00000368024.5:p.Arg318Thr
|
|
ENST00000241041.7:c.953-135G>C
|
ENSP00000241041.3:n.953-135G>C
|
|
ENST00000378750.9:c.953G>C
|
ENSP00000368024.5:p.Arg318Thr
|
|
ENST00000523721.2:n.183G>C
|
|
|
ENST00000532681.5:c.668G>C
|
ENSP00000434654.1:p.Arg223Thr
|
|
NM_004813.2:c.953G>C
|
NP_004804.1:p.Arg318Thr
|
|
NM_057174.2:c.953-135G>C
|
NP_476515.1:n.953-135G>C
|
|
XM_011520474.1:c.830G>C
|
XP_011518776.1:p.Arg277Thr
|
|
NM_004813.3:c.953G>C
|
NP_004804.1:p.Arg318Thr
|
|
NM_004813.4:c.953G>C
MANE Select
|
NP_004804.2:p.Arg318Thr
|
|
NM_057174.3:c.953-135G>C
|
NP_476515.2:n.953-135G>C
|
|