ENST00000696170.1:c.*417A>T
|
ENSP00000512461.1:n.*417A>T
|
|
ENST00000696171.1:c.812A>T
|
ENSP00000512462.1:p.His271Leu
|
|
ENST00000378588.5:c.908A>T
MANE Select
|
ENSP00000367851.4:p.His303Leu
|
|
ENST00000378588.4:c.908A>T
|
ENSP00000367851.4:p.His303Leu
|
|
ENST00000465127.1:c.171+377887A>T
|
ENSP00000417050.1:n.171+377887A>T
|
|
ENST00000492288.1:n.333A>T
|
|
|
NM_000397.3:c.908A>T , LRG_53t1:c.908A>T
|
NP_000388.2:p.His303Leu
|
|
XM_011543890.1:c.602A>T
|
XP_011542192.1:p.His201Leu
|
|
NM_000397.4:c.908A>T
MANE Select
|
NP_000388.2:p.His303Leu
|
|