ENST00000644269.2:c.1455G>C
MANE Select
|
ENSP00000494017.1:p.Thr485=
|
|
ENST00000644846.1:c.166G>C
|
|
|
ENST00000265715.7:c.1455G>C
|
ENSP00000265715.3:p.Thr485=
|
|
ENST00000460748.1:n.558G>C
|
|
|
ENST00000477350.5:n.302G>C
|
|
|
ENST00000480841.5:n.304G>C
|
|
|
ENST00000497446.5:n.470G>C
|
|
|
NM_000441.1:c.1455G>C
|
NP_000432.1:p.Thr485=
|
|
XM_005250425.1:c.1455G>C
|
XP_005250482.1:p.Thr485=
|
|
XM_005250425.2:c.1455G>C
|
XP_005250482.1:p.Thr485=
|
|
XM_017012318.1:c.1377G>C
|
XP_016867807.1:p.Thr459=
|
|
NM_000441.2:c.1455G>C
MANE Select
|
NP_000432.1:p.Thr485=
|
|