ENST00000405440.7:c.141C>A
MANE Select
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ENSP00000384152.3:p.Thr47=
|
|
ENST00000310346.8:c.141C>A
|
ENSP00000309913.4:p.Thr47=
|
|
ENST00000349716.9:c.-3-1838C>A
|
ENSP00000337723.5:n.-3-1838C>A
|
|
ENST00000405440.6:c.141C>A
|
ENSP00000384152.2:p.Thr47=
|
|
ENST00000526441.1:c.141C>A
|
ENSP00000433292.1:p.Thr47=
|
|
ENST00000552726.1:n.192C>A
|
|
|
NM_000192.3:c.141C>A , LRG_670t1:c.141C>A
|
NP_000183.2:p.Thr47=
|
|
NM_080717.2:c.-3-1838C>A
|
NP_542448.1:n.-3-1838C>A
|
|
NM_181486.2:c.141C>A
|
NP_852259.1:p.Thr47=
|
|
XM_017019912.1:c.189C>A
|
XP_016875401.1:p.Thr63=
|
|
NM_080717.3:c.-3-1838C>A
|
NP_542448.1:n.-3-1838C>A
|
|
NM_181486.4:c.141C>A
MANE Select
|
NP_852259.1:p.Thr47=
|
|
NM_080717.4:c.-3-1838C>A
|
NP_542448.1:n.-3-1838C>A
|
|