ENST00000696170.1:c.*51T=
|
ENSP00000512461.1:n.*51T=
|
|
ENST00000696171.1:c.446T=
|
ENSP00000512462.1:p.Val149=
|
|
ENST00000696172.1:c.338-2946T=
|
ENSP00000512463.1:n.338-2946T=
|
|
ENST00000378588.5:c.542T=
MANE Select
|
ENSP00000367851.4:p.Val181=
|
|
ENST00000378588.4:c.542T=
|
ENSP00000367851.4:p.Val181=
|
|
ENST00000465127.1:c.171+370009T=
|
ENSP00000417050.1:n.171+370009T=
|
|
NM_000397.3:c.542T= , LRG_53t1:c.542T=
|
NP_000388.2:p.Val181=
|
|
XM_011543890.1:c.236T=
|
XP_011542192.1:p.Val79=
|
|
NM_000397.4:c.542T=
MANE Select
|
NP_000388.2:p.Val181=
|
|