ENST00000475778.2:n.719T>C
|
|
|
ENST00000683214.1:n.544+14032T>C
|
|
|
ENST00000684143.1:c.293T>C
|
ENSP00000508264.1:p.Met98Thr
|
|
ENST00000379374.5:c.293T>C
MANE Select
|
ENSP00000368682.4:p.Met98Thr
|
|
ENST00000379374.4:c.293T>C
|
ENSP00000368682.4:p.Met98Thr
|
|
NM_000444.5:c.293T>C
|
NP_000435.3:p.Met98Thr
|
|
NM_001282754.1:c.293T>C
|
NP_001269683.1:p.Met98Thr
|
|
XM_011545535.1:c.293T>C
|
XP_011543837.1:p.Met98Thr
|
|
XM_024452390.1:c.2T>C
|
XP_024308158.1:p.Met1Thr
|
|
XR_001755695.1:n.972T>C
|
|
|
NM_000444.6:c.293T>C
MANE Select
|
NP_000435.3:p.Met98Thr
|
|
NM_001282754.2:c.293T>C
|
NP_001269683.1:p.Met98Thr
|
|