ENST00000682565.1:c.7680T>C
|
ENSP00000507671.1:p.Ala2560=
|
|
ENST00000682801.1:c.7680T>C
|
ENSP00000507862.1:p.Ala2560=
|
|
ENST00000682859.1:c.7680T>C
|
ENSP00000508222.1:p.Ala2560=
|
|
ENST00000683791.1:c.1072T>C
|
|
|
ENST00000684460.1:c.5132T>C
|
|
|
ENST00000684548.1:c.7680T>C
|
ENSP00000507421.1:p.Ala2560=
|
|
ENST00000684590.1:c.2127T>C
|
ENSP00000507376.1:p.Ala709=
|
|
ENST00000684656.1:c.5132T>C
|
|
|
ENST00000613296.6:c.8061T>C
MANE Select
|
ENSP00000482968.1:p.Ala2687=
|
|
ENST00000651434.1:c.896-29755T>C
|
|
|
ENST00000423048.5:c.2892T>C
|
ENSP00000399833.1:p.Ala964=
|
|
ENST00000484298.5:c.7935T>C
|
ENSP00000478155.1:p.Ala2645=
|
|
ENST00000613296.4:c.8061T>C
|
ENSP00000482968.1:p.Ala2687=
|
|
ENST00000614410.4:c.8061T>C
|
ENSP00000479094.1:p.Ala2687=
|
|
ENST00000620466.4:n.1864T>C
|
|
|
NM_015120.4:c.8064T>C , LRG_741t1:c.8064T>C
|
NP_055935.4:p.Ala2688=
|
|
NM_001378454.1:c.8061T>C
MANE Select
|
NP_001365383.1:p.Ala2687=
|
|