ENST00000475778.2:n.1268T>C
|
|
|
ENST00000684143.1:c.839T>C
|
ENSP00000508264.1:p.Ile280Thr
|
|
ENST00000684745.1:n.516T>C
|
|
|
ENST00000379374.5:c.842T>C
MANE Select
|
ENSP00000368682.4:p.Ile281Thr
|
|
ENST00000379374.4:c.842T>C
|
ENSP00000368682.4:p.Ile281Thr
|
|
ENST00000475778.1:n.115T>C
|
|
|
NM_000444.5:c.842T>C
|
NP_000435.3:p.Ile281Thr
|
|
NM_001282754.1:c.842T>C
|
NP_001269683.1:p.Ile281Thr
|
|
XM_011545533.1:c.86T>C
|
XP_011543835.1:p.Ile29Thr
|
|
XM_011545534.1:c.86T>C
|
XP_011543836.1:p.Ile29Thr
|
|
XM_011545535.1:c.842T>C
|
XP_011543837.1:p.Ile281Thr
|
|
XM_017029579.1:c.86T>C
|
XP_016885068.1:p.Ile29Thr
|
|
XM_024452390.1:c.551T>C
|
XP_024308158.1:p.Ile184Thr
|
|
XR_001755695.1:n.1521T>C
|
|
|
NM_000444.6:c.842T>C
MANE Select
|
NP_000435.3:p.Ile281Thr
|
|
NM_001282754.2:c.842T>C
|
NP_001269683.1:p.Ile281Thr
|
|