ENST00000281928.9:c.5601T>C
MANE Select
|
ENSP00000281928.3:p.Ser1867=
|
|
ENST00000548694.2:n.591T>C
|
|
|
ENST00000648379.1:n.3969T>C
|
|
|
ENST00000648737.1:n.5365T>C
|
|
|
ENST00000648825.1:n.3786T>C
|
|
|
ENST00000648916.1:n.3612T>C
|
|
|
ENST00000649607.1:c.3785T>C
|
|
|
ENST00000649775.1:c.2090T>C
|
|
|
ENST00000650226.1:c.5637T>C
|
ENSP00000496981.1:p.Ser1879=
|
|
ENST00000281928.7:c.5601T>C
|
ENSP00000281928.3:p.Ser1867=
|
|
ENST00000548694.1:n.591T>C
|
|
|
ENST00000552447.1:c.214T>C
|
|
|
NM_015335.4:c.5601T>C
|
NP_056150.1:p.Ser1867=
|
|
XM_011538080.1:c.5637T>C
|
XP_011536382.1:p.Ser1879=
|
|
XM_011538081.1:c.5634T>C
|
XP_011536383.1:p.Ser1878=
|
|
XM_011538082.1:c.5607T>C
|
XP_011536384.1:p.Ser1869=
|
|
XM_011538080.2:c.5637T>C
|
XP_011536382.1:p.Ser1879=
|
|
XM_011538081.2:c.5634T>C
|
XP_011536383.1:p.Ser1878=
|
|
XM_011538082.2:c.5607T>C
|
XP_011536384.1:p.Ser1869=
|
|
XM_017019090.1:c.5598T>C
|
XP_016874579.1:p.Ser1866=
|
|
NM_015335.5:c.5601T>C
MANE Select
|
NP_056150.1:p.Ser1867=
|
|