ENST00000265512.12:c.970T>G
MANE Select
|
ENSP00000265512.7:p.Phe324Val
|
|
ENST00000265512.11:c.970T>G
|
ENSP00000265512.7:p.Phe324Val
|
|
ENST00000505590.5:c.1027T>G
|
ENSP00000425416.1:p.Phe343Val
|
|
ENST00000506705.5:c.*944T>G
|
ENSP00000426667.1:n.*944T>G
|
|
ENST00000508393.5:c.1027T>G
|
ENSP00000424630.1:p.Phe343Val
|
|
ENST00000509471.5:c.334-486T>G
|
ENSP00000424583.1:n.334-486T>G
|
|
ENST00000629236.2:c.970T>G
|
ENSP00000486450.1:p.Phe324Val
|
|
NM_000670.3:c.970T>G
|
NP_000661.2:p.Phe324Val
|
|
NM_000670.4:c.970T>G
|
NP_000661.2:p.Phe324Val
|
|
NM_001306171.1:c.1027T>G
|
NP_001293100.1:p.Phe343Val
|
|
NM_001306172.1:c.1027T>G
|
NP_001293101.1:p.Phe343Val
|
|
NR_037884.1:n.429-6337A>C
|
|
|
XR_938685.1:n.1198T>G
|
|
|
XR_938686.1:n.1189T>G
|
|
|
XR_938687.1:n.1062T>G
|
|
|
NM_000670.5:c.970T>G
MANE Select
|
NP_000661.2:p.Phe324Val
|
|
NM_001306171.2:c.1027T>G
|
NP_001293100.1:p.Phe343Val
|
|
NM_001306172.2:c.1027T>G
|
NP_001293101.1:p.Phe343Val
|
|