ENST00000624552.4:c.14889G>C
|
ENSP00000485357.2:p.Thr4963=
|
|
ENST00000683500.2:c.14946G>C
MANE Select
|
ENSP00000508292.2:p.Thr4982=
|
|
ENST00000623487.1:n.3292G>C
|
|
|
ENST00000624552.3:c.14886G>C
|
ENSP00000485357.1:p.Thr4962=
|
|
NM_001291815.1:c.14946G>C
|
NP_001278744.1:p.Thr4982=
|
|
XM_011518465.1:c.14823G>C
|
XP_011516767.1:p.Thr4941=
|
|
XM_011518466.1:c.14814G>C
|
XP_011516768.1:p.Thr4938=
|
|
XM_011518467.1:c.14769G>C
|
XP_011516769.1:p.Thr4923=
|
|
NM_001291815.2:c.14946G>C
MANE Select
|
NP_001278744.1:p.Thr4982=
|
|
XM_011518465.2:c.14823G>C
|
XP_011516767.1:p.Thr4941=
|
|
XM_011518466.2:c.14814G>C
|
XP_011516768.1:p.Thr4938=
|
|
XM_011518467.2:c.14769G>C
|
XP_011516769.1:p.Thr4923=
|
|
XM_017014585.1:c.11727G>C
|
XP_016870074.1:p.Thr3909=
|
|
XM_017014586.1:c.7524G>C
|
XP_016870075.1:p.Thr2508=
|
|
XR_001746957.1:n.92+222C>G
|
|
|
XR_001746958.1:n.92+222C>G
|
|
|