ENST00000696170.1:c.*534T>G
|
ENSP00000512461.1:n.*534T>G
|
|
ENST00000696171.1:c.929T>G
|
ENSP00000512462.1:p.Leu310Arg
|
|
ENST00000378588.5:c.1025T>G
MANE Select
|
ENSP00000367851.4:p.Leu342Arg
|
|
ENST00000378588.4:c.1025T>G
|
ENSP00000367851.4:p.Leu342Arg
|
|
ENST00000465127.1:c.171+378004T>G
|
ENSP00000417050.1:n.171+378004T>G
|
|
ENST00000492288.1:n.450T>G
|
|
|
NM_000397.3:c.1025T>G , LRG_53t1:c.1025T>G
|
NP_000388.2:p.Leu342Arg
|
|
XM_011543890.1:c.719T>G
|
XP_011542192.1:p.Leu240Arg
|
|
NM_000397.4:c.1025T>G
MANE Select
|
NP_000388.2:p.Leu342Arg
|
|