ENST00000695651.1:n.2638C>T
|
|
|
ENST00000695653.1:c.2199C>T
|
ENSP00000512084.1:p.Ser733=
|
|
ENST00000695654.1:c.3315C>T
|
ENSP00000512085.1:p.Ser1105=
|
|
ENST00000695689.1:c.261C>T
|
ENSP00000512101.1:n.261C>T
|
|
ENST00000695690.1:n.481C>T
|
|
|
ENST00000695691.1:n.481C>T
|
|
|
ENST00000245907.11:c.4290C>T
MANE Select
|
ENSP00000245907.4:p.Ser1430=
|
|
ENST00000245907.10:c.4290C>T
|
ENSP00000245907.4:p.Ser1430=
|
|
ENST00000596548.1:c.411C>T
|
ENSP00000469744.1:p.Ser137=
|
|
ENST00000599899.5:n.1249C>T
|
|
|
ENST00000601008.1:c.242-4043C>T
|
ENSP00000471384.1:n.242-4043C>T
|
|
NM_000064.3:c.4290C>T
|
NP_000055.2:p.Ser1430=
|
|
NM_000064.4:c.4290C>T
MANE Select
|
NP_000055.2:p.Ser1430=
|
|