ENST00000548747.6:c.1971T>C
MANE Select
|
ENSP00000448828.1:p.Ser657=
|
|
ENST00000449260.6:c.1992T>C
|
ENSP00000402758.2:p.Ser664=
|
|
ENST00000548493.5:c.1971T>C
|
ENSP00000447374.1:p.Ser657=
|
|
ENST00000548747.5:c.1971T>C
|
ENSP00000448828.1:p.Ser657=
|
|
ENST00000550447.5:c.858T>C
|
ENSP00000448029.1:p.Ser286=
|
|
ENST00000550464.5:c.1713T>C
|
ENSP00000450036.1:p.Ser571=
|
|
ENST00000552882.5:c.1971T>C
|
ENSP00000449690.1:p.Ser657=
|
|
NM_001200053.1:c.1713T>C
|
NP_001186982.1:p.Ser571=
|
|
NM_001200054.1:c.1992T>C
|
NP_001186983.1:p.Ser664=
|
|
NM_006928.4:c.1971T>C
|
NP_008859.1:p.Ser657=
|
|
XM_006719569.1:c.1971T>C
|
XP_006719632.1:p.Ser657=
|
|
XM_011538685.1:c.1992T>C
|
XP_011536987.1:p.Ser664=
|
|
XM_011538686.1:c.1866T>C
|
XP_011536988.1:p.Ser622=
|
|
XM_011538687.1:c.1845T>C
|
XP_011536989.1:p.Ser615=
|
|
NM_001320121.1:c.1866T>C
|
NP_001307050.1:p.Ser622=
|
|
NM_001320122.1:c.1845T>C
|
NP_001307051.1:p.Ser615=
|
|
NM_001384361.1:c.1971T>C
MANE Select
|
NP_001371290.1:p.Ser657=
|
|
NM_006928.5:c.1971T>C
|
NP_008859.1:p.Ser657=
|
|