|
NM_003860.4:c.9C>T
MANE Select
|
NP_003851.1:p.Thr3=
|
|
ENST00000312175.7:c.9C>T
MANE Select
|
ENSP00000310275.2:p.Thr3=
|
|
NM_001143985.1:c.9C>T
|
NP_001137457.1:p.Thr3=
|
|
NM_003860.3:c.9C>T
|
NP_003851.1:p.Thr3=
|
|
ENST00000312175.6:c.9C>T
|
ENSP00000310275.2:p.Thr3=
|
|
ENST00000445560.6:c.9C>T
|
ENSP00000416128.2:p.Thr3=
|
|
ENST00000524628.1:n.92-367C>T
|
|
|
ENST00000524663.1:n.199-367C>T
|
|
|
ENST00000527348.1:c.9C>T
|
ENSP00000432867.1:p.Thr3=
|
|
ENST00000528648.1:n.24C>T
|
|
|
ENST00000530204.1:c.9C>T
|
ENSP00000431785.1:p.Thr3=
|
|
ENST00000533166.5:c.9C>T
|
ENSP00000433760.1:p.Thr3=
|
|
XM_017018514.1:c.9C>T
|
XP_016874003.1:p.Thr3=
|
|
XM_017018515.2:c.9C>T
|
XP_016874004.1:p.Thr3=
|