ENST00000548747.6:c.1855A>C
MANE Select
|
ENSP00000448828.1:p.Arg619=
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|
ENST00000449260.6:c.1876A>C
|
ENSP00000402758.2:p.Arg626=
|
|
ENST00000548493.5:c.1855A>C
|
ENSP00000447374.1:p.Arg619=
|
|
ENST00000548747.5:c.1855A>C
|
ENSP00000448828.1:p.Arg619=
|
|
ENST00000549564.1:n.434A>C
|
|
|
ENST00000550447.5:c.742A>C
|
ENSP00000448029.1:p.Arg248=
|
|
ENST00000550464.5:c.1597A>C
|
ENSP00000450036.1:p.Arg533=
|
|
ENST00000552882.5:c.1855A>C
|
ENSP00000449690.1:p.Arg619=
|
|
NM_001200053.1:c.1597A>C
|
NP_001186982.1:p.Arg533=
|
|
NM_001200054.1:c.1876A>C
|
NP_001186983.1:p.Arg626=
|
|
NM_006928.4:c.1855A>C
|
NP_008859.1:p.Arg619=
|
|
XM_006719569.1:c.1855A>C
|
XP_006719632.1:p.Arg619=
|
|
XM_011538685.1:c.1876A>C
|
XP_011536987.1:p.Arg626=
|
|
XM_011538686.1:c.1750A>C
|
XP_011536988.1:p.Arg584=
|
|
XM_011538687.1:c.1729A>C
|
XP_011536989.1:p.Arg577=
|
|
NM_001320121.1:c.1750A>C
|
NP_001307050.1:p.Arg584=
|
|
NM_001320122.1:c.1729A>C
|
NP_001307051.1:p.Arg577=
|
|
NM_001384361.1:c.1855A>C
MANE Select
|
NP_001371290.1:p.Arg619=
|
|
NM_006928.5:c.1855A>C
|
NP_008859.1:p.Arg619=
|
|