ENST00000265512.12:c.974T>C
MANE Select
|
ENSP00000265512.7:p.Phe325Ser
|
|
ENST00000265512.11:c.974T>C
|
ENSP00000265512.7:p.Phe325Ser
|
|
ENST00000505590.5:c.1031T>C
|
ENSP00000425416.1:p.Phe344Ser
|
|
ENST00000506705.5:c.*948T>C
|
ENSP00000426667.1:n.*948T>C
|
|
ENST00000508393.5:c.1031T>C
|
ENSP00000424630.1:p.Phe344Ser
|
|
ENST00000509471.5:c.334-482T>C
|
ENSP00000424583.1:n.334-482T>C
|
|
ENST00000629236.2:c.974T>C
|
ENSP00000486450.1:p.Phe325Ser
|
|
NM_000670.3:c.974T>C
|
NP_000661.2:p.Phe325Ser
|
|
NM_000670.4:c.974T>C
|
NP_000661.2:p.Phe325Ser
|
|
NM_001306171.1:c.1031T>C
|
NP_001293100.1:p.Phe344Ser
|
|
NM_001306172.1:c.1031T>C
|
NP_001293101.1:p.Phe344Ser
|
|
NR_037884.1:n.429-6341A>G
|
|
|
XR_938685.1:n.1202T>C
|
|
|
XR_938686.1:n.1193T>C
|
|
|
XR_938687.1:n.1066T>C
|
|
|
NM_000670.5:c.974T>C
MANE Select
|
NP_000661.2:p.Phe325Ser
|
|
NM_001306171.2:c.1031T>C
|
NP_001293100.1:p.Phe344Ser
|
|
NM_001306172.2:c.1031T>C
|
NP_001293101.1:p.Phe344Ser
|
|