ENST00000695651.1:n.1086A>T
|
|
|
ENST00000695652.1:c.2615A>T
|
ENSP00000512083.1:p.Lys872Met
|
|
ENST00000695653.1:c.647A>T
|
ENSP00000512084.1:p.Lys216Met
|
|
ENST00000695654.1:c.1862A>T
|
ENSP00000512085.1:p.Lys621Met
|
|
ENST00000695655.1:c.1679A>T
|
ENSP00000512086.1:n.1679A>T
|
|
ENST00000695692.1:n.2102A>T
|
|
|
ENST00000245907.11:c.2738A>T
MANE Select
|
ENSP00000245907.4:p.Lys913Met
|
|
ENST00000245907.10:c.2738A>T
|
ENSP00000245907.4:p.Lys913Met
|
|
ENST00000594005.1:n.314A>T
|
|
|
NM_000064.3:c.2738A>T
|
NP_000055.2:p.Lys913Met
|
|
NM_000064.4:c.2738A>T
MANE Select
|
NP_000055.2:p.Lys913Met
|
|