ENST00000381944.5:c.*451G>T
|
ENSP00000371370.3:n.*451G>T
|
|
ENST00000473664.2:c.731G>T
|
ENSP00000502741.1:p.Arg244Leu
|
|
ENST00000488495.3:c.1237G>T
|
ENSP00000494009.1:p.Val413Phe
|
|
ENST00000645534.1:c.1237G>T
MANE Select
|
ENSP00000494193.1:p.Val413Phe
|
|
ENST00000217254.11:c.1237G>T
|
ENSP00000217254.7:p.Val413Phe
|
|
ENST00000381944.4:c.*451G>T
|
ENSP00000371370.3:n.*451G>T
|
|
ENST00000473664.1:n.782G>T
|
|
|
ENST00000632431.1:c.1237G>T
|
ENSP00000488723.1:p.Val413Phe
|
|
NM_033409.3:c.1237G>T
|
NP_212134.3:p.Val413Phe
|
|
XM_005260655.3:c.1237G>T
|
XP_005260712.1:p.Val413Phe
|
|
XM_011529148.1:c.1237G>T
|
XP_011527450.1:p.Val413Phe
|
|
XM_005260655.4:c.1237G>T
|
XP_005260712.1:p.Val413Phe
|
|
XM_024451821.1:c.1237G>T
|
XP_024307589.1:p.Val413Phe
|
|
NM_033409.4:c.1237G>T
MANE Select
|
NP_212134.3:p.Val413Phe
|
|
NM_001370085.1:c.1237G>T
|
NP_001357014.1:p.Val413Phe
|
|
NM_001370086.1:c.1237G>T
|
NP_001357015.1:p.Val413Phe
|
|