ENST00000295897.9:c.1432T>G
MANE Select
|
ENSP00000295897.4:p.Ser478Ala
|
|
ENST00000295897.8:c.1432T>G
|
ENSP00000295897.4:p.Ser478Ala
|
|
ENST00000401494.7:c.1087T>G
|
ENSP00000384695.3:p.Ser363Ala
|
|
ENST00000415165.6:c.856T>G
|
ENSP00000401820.2:p.Ser286Ala
|
|
ENST00000476441.6:c.*711T>G
|
ENSP00000423727.1:n.*711T>G
|
|
ENST00000486939.1:n.86T>G
|
|
|
ENST00000503124.5:c.982T>G
|
ENSP00000421027.1:p.Ser328Ala
|
|
ENST00000505649.5:n.979T>G
|
|
|
ENST00000509063.5:c.1432T>G
|
ENSP00000422784.1:p.Ser478Ala
|
|
ENST00000511370.1:c.965T>G
|
|
|
ENST00000621085.4:c.793T>G
|
ENSP00000483421.1:p.Ser265Ala
|
|
ENST00000621628.4:c.793T>G
|
ENSP00000480485.1:p.Ser265Ala
|
|
NM_000477.5:c.1432T>G
|
NP_000468.1:p.Ser478Ala
|
|
NM_000477.6:c.1432T>G
|
NP_000468.1:p.Ser478Ala
|
|
NM_000477.7:c.1432T>G
MANE Select
|
NP_000468.1:p.Ser478Ala
|
|