ENST00000695651.1:n.2610T>G
|
|
|
ENST00000695653.1:c.2171T>G
|
ENSP00000512084.1:p.Leu724Arg
|
|
ENST00000695654.1:c.3287T>G
|
ENSP00000512085.1:p.Leu1096Arg
|
|
ENST00000695689.1:c.233T>G
|
ENSP00000512101.1:n.233T>G
|
|
ENST00000695690.1:n.453T>G
|
|
|
ENST00000695691.1:n.453T>G
|
|
|
ENST00000245907.11:c.4262T>G
MANE Select
|
ENSP00000245907.4:p.Leu1421Arg
|
|
ENST00000245907.10:c.4262T>G
|
ENSP00000245907.4:p.Leu1421Arg
|
|
ENST00000596548.1:c.383T>G
|
ENSP00000469744.1:p.Leu128Arg
|
|
ENST00000599899.5:n.1221T>G
|
|
|
ENST00000601008.1:c.242-4071T>G
|
ENSP00000471384.1:n.242-4071T>G
|
|
NM_000064.3:c.4262T>G
|
NP_000055.2:p.Leu1421Arg
|
|
NM_000064.4:c.4262T>G
MANE Select
|
NP_000055.2:p.Leu1421Arg
|
|