ENST00000703783.1:n.1030A>T
|
|
|
ENST00000703785.1:n.1111A>T
|
|
|
ENST00000262464.9:c.4246A>T
MANE Select
|
ENSP00000262464.4:p.Thr1416Ser
|
|
ENST00000262464.8:c.4246A>T
|
ENSP00000262464.4:p.Thr1416Ser
|
|
ENST00000507835.5:c.796A>T
|
ENSP00000426839.1:p.Thr266Ser
|
|
ENST00000508053.5:c.4246A>T
|
ENSP00000424571.1:p.Thr1416Ser
|
|
ENST00000508989.5:c.4147A>T
|
ENSP00000425596.1:p.Thr1383Ser
|
|
ENST00000619499.4:c.4243A>T
|
ENSP00000482132.1:p.Thr1415Ser
|
|
NM_001999.3:c.4246A>T
|
NP_001990.2:p.Thr1416Ser
|
|
XM_017009228.2:c.4093A>T
|
XP_016864717.1:p.Thr1365Ser
|
|
NM_001999.4:c.4246A>T
MANE Select
|
NP_001990.2:p.Thr1416Ser
|
|