ENST00000576204.6:n.820T>A
|
|
|
ENST00000622290.5:c.*129T>A
|
ENSP00000483331.2:n.*129T>A
|
|
ENST00000205557.12:c.3957T>A
MANE Select
|
ENSP00000205557.7:p.Ala1319=
|
|
ENST00000640696.1:c.771T>A
|
ENSP00000492197.1:p.Ala257=
|
|
ENST00000205557.11:c.3957T>A
|
ENSP00000205557.7:p.Ala1319=
|
|
ENST00000456970.6:c.3582T>A
|
ENSP00000405002.2:n.3582T>A
|
|
ENST00000576204.5:n.820T>A
|
|
|
ENST00000622290.4:c.*1166T>A
|
ENSP00000483331.1:n.*1166T>A
|
|
NM_001171.5:c.3957T>A
|
NP_001162.4:p.Ala1319=
|
|
XM_011522479.1:c.3924T>A
|
XP_011520781.1:p.Ala1308=
|
|
XM_011522480.1:c.3615T>A
|
XP_011520782.1:p.Ala1205=
|
|
XM_011522481.1:c.3615T>A
|
XP_011520783.1:p.Ala1205=
|
|
XR_932836.1:n.4255T>A
|
|
|
XR_932837.1:n.3993T>A
|
|
|
XR_932838.1:n.4056T>A
|
|
|
XR_933134.1:n.539-4824A>T
|
|
|
NM_001351800.1:c.3615T>A
|
NP_001338729.1:p.Ala1205=
|
|
NR_147784.1:n.3619T>A
|
|
|
XM_011522479.2:c.3924T>A
|
XP_011520781.1:p.Ala1308=
|
|
XM_011522481.3:c.3615T>A
|
XP_011520783.1:p.Ala1205=
|
|
XM_017023212.1:c.3789T>A
|
XP_016878701.1:p.Ala1263=
|
|
XM_024450261.1:c.3993T>A
|
XP_024306029.1:p.Ala1331=
|
|
XR_932837.3:n.3938T>A
|
|
|
NM_001171.6:c.3957T>A
MANE Select
|
NP_001162.5:p.Ala1319=
|
|