ENST00000243964.7:c.2881G=
MANE Select
|
ENSP00000243964.4:p.Gly961=
|
|
ENST00000243964.6:c.2881G=
|
ENSP00000243964.3:p.Gly961=
|
|
ENST00000454036.6:c.2950G=
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ENSP00000387694.1:p.Gly984=
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|
ENST00000616201.4:c.1298-2413G=
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ENSP00000484585.1:n.1298-2413G=
|
|
ENST00000616202.4:c.613-2238G=
|
ENSP00000478369.1:n.613-2238G=
|
|
ENST00000616933.4:c.*2199G=
|
ENSP00000477569.1:n.*2199G=
|
|
ENST00000626937.2:c.510-3356G=
|
ENSP00000485953.1:n.510-3356G=
|
|
ENST00000628413.1:n.397G=
|
|
|
NM_001134771.1:c.2950G=
|
NP_001128243.1:p.Gly984=
|
|
NM_020708.4:c.2881G=
|
NP_065759.1:p.Gly961=
|
|
XM_017027981.1:c.2950G=
|
XP_016883470.1:p.Gly984=
|
|
NM_001134771.2:c.2950G=
|
NP_001128243.1:p.Gly984=
|
|
NM_020708.5:c.2881G=
MANE Select
|
NP_065759.1:p.Gly961=
|
|