ENST00000682565.1:c.7335T>G
|
ENSP00000507671.1:p.Ala2445=
|
|
ENST00000682801.1:c.7335T>G
|
ENSP00000507862.1:p.Ala2445=
|
|
ENST00000682859.1:c.7335T>G
|
ENSP00000508222.1:p.Ala2445=
|
|
ENST00000683791.1:c.727T>G
|
|
|
ENST00000684460.1:c.4787T>G
|
|
|
ENST00000684548.1:c.7335T>G
|
ENSP00000507421.1:p.Ala2445=
|
|
ENST00000684590.1:c.1782T>G
|
ENSP00000507376.1:p.Ala594=
|
|
ENST00000684656.1:c.4787T>G
|
|
|
ENST00000613296.6:c.7716T>G
MANE Select
|
ENSP00000482968.1:p.Ala2572=
|
|
ENST00000651434.1:c.896-30100T>G
|
|
|
ENST00000423048.5:c.2547T>G
|
ENSP00000399833.1:p.Ala849=
|
|
ENST00000484298.5:c.7590T>G
|
ENSP00000478155.1:p.Ala2530=
|
|
ENST00000613296.4:c.7716T>G
|
ENSP00000482968.1:p.Ala2572=
|
|
ENST00000614410.4:c.7716T>G
|
ENSP00000479094.1:p.Ala2572=
|
|
ENST00000620466.4:n.1519T>G
|
|
|
NM_015120.4:c.7719T>G , LRG_741t1:c.7719T>G
|
NP_055935.4:p.Ala2573=
|
|
NM_001378454.1:c.7716T>G
MANE Select
|
NP_001365383.1:p.Ala2572=
|
|