ENST00000281928.9:c.5949T>C
MANE Select
|
ENSP00000281928.3:p.Ser1983=
|
|
ENST00000548784.2:n.2163T>C
|
|
|
ENST00000648379.1:n.4317T>C
|
|
|
ENST00000648737.1:n.5713T>C
|
|
|
ENST00000648825.1:n.4134T>C
|
|
|
ENST00000648916.1:n.3960T>C
|
|
|
ENST00000649607.1:c.4133T>C
|
|
|
ENST00000649775.1:c.2438T>C
|
|
|
ENST00000650226.1:c.5985T>C
|
ENSP00000496981.1:p.Ser1995=
|
|
ENST00000281928.7:c.5949T>C
|
ENSP00000281928.3:p.Ser1983=
|
|
ENST00000548784.1:n.447T>C
|
|
|
ENST00000552447.1:c.562T>C
|
|
|
NM_015335.4:c.5949T>C
|
NP_056150.1:p.Ser1983=
|
|
XM_011538080.1:c.5985T>C
|
XP_011536382.1:p.Ser1995=
|
|
XM_011538081.1:c.5982T>C
|
XP_011536383.1:p.Ser1994=
|
|
XM_011538082.1:c.5955T>C
|
XP_011536384.1:p.Ser1985=
|
|
XM_011538080.2:c.5985T>C
|
XP_011536382.1:p.Ser1995=
|
|
XM_011538081.2:c.5982T>C
|
XP_011536383.1:p.Ser1994=
|
|
XM_011538082.2:c.5955T>C
|
XP_011536384.1:p.Ser1985=
|
|
XM_017019090.1:c.5946T>C
|
XP_016874579.1:p.Ser1982=
|
|
NM_015335.5:c.5949T>C
MANE Select
|
NP_056150.1:p.Ser1983=
|
|