ENST00000696170.1:c.*49T>C
|
ENSP00000512461.1:n.*49T>C
|
|
ENST00000696171.1:c.444T>C
|
ENSP00000512462.1:p.Val148=
|
|
ENST00000696172.1:c.338-2948T>C
|
ENSP00000512463.1:n.338-2948T>C
|
|
ENST00000378588.5:c.540T>C
MANE Select
|
ENSP00000367851.4:p.Val180=
|
|
ENST00000378588.4:c.540T>C
|
ENSP00000367851.4:p.Val180=
|
|
ENST00000465127.1:c.171+370007T>C
|
ENSP00000417050.1:n.171+370007T>C
|
|
NM_000397.3:c.540T>C , LRG_53t1:c.540T>C
|
NP_000388.2:p.Val180=
|
|
XM_011543890.1:c.234T>C
|
XP_011542192.1:p.Val78=
|
|
NM_000397.4:c.540T>C
MANE Select
|
NP_000388.2:p.Val180=
|
|