ENST00000624552.4:c.14888C>G
|
ENSP00000485357.2:p.Thr4963Arg
|
|
ENST00000683500.2:c.14945C>G
MANE Select
|
ENSP00000508292.2:p.Thr4982Arg
|
|
ENST00000623487.1:n.3291C>G
|
|
|
ENST00000624552.3:c.14885C>G
|
ENSP00000485357.1:p.Thr4962Arg
|
|
NM_001291815.1:c.14945C>G
|
NP_001278744.1:p.Thr4982Arg
|
|
XM_011518465.1:c.14822C>G
|
XP_011516767.1:p.Thr4941Arg
|
|
XM_011518466.1:c.14813C>G
|
XP_011516768.1:p.Thr4938Arg
|
|
XM_011518467.1:c.14768C>G
|
XP_011516769.1:p.Thr4923Arg
|
|
NM_001291815.2:c.14945C>G
MANE Select
|
NP_001278744.1:p.Thr4982Arg
|
|
XM_011518465.2:c.14822C>G
|
XP_011516767.1:p.Thr4941Arg
|
|
XM_011518466.2:c.14813C>G
|
XP_011516768.1:p.Thr4938Arg
|
|
XM_011518467.2:c.14768C>G
|
XP_011516769.1:p.Thr4923Arg
|
|
XM_017014585.1:c.11726C>G
|
XP_016870074.1:p.Thr3909Arg
|
|
XM_017014586.1:c.7523C>G
|
XP_016870075.1:p.Thr2508Arg
|
|
XR_001746957.1:n.92+223G>C
|
|
|
XR_001746958.1:n.92+223G>C
|
|
|