ENST00000302450.11:c.815T>C
MANE Select
|
ENSP00000305204.6:p.Val272Ala
|
|
ENST00000302450.10:c.815T>C
|
ENSP00000305204.6:p.Val272Ala
|
|
ENST00000435431.5:c.478+337T>C
|
ENSP00000414834.1:n.478+337T>C
|
|
NM_001304361.1:c.320T>C
|
NP_001291290.1:p.Val107Ala
|
|
NM_152515.4:c.815T>C
|
NP_689728.3:p.Val272Ala
|
|
NR_130712.1:n.557+337T>C
|
|
|
XM_011510666.1:c.320T>C
|
XP_011508968.1:p.Val107Ala
|
|
XM_011510666.2:c.320T>C
|
XP_011508968.1:p.Val107Ala
|
|
NM_152515.5:c.815T>C
MANE Select
|
NP_689728.3:p.Val272Ala
|
|
NM_001304361.2:c.320T>C
|
NP_001291290.1:p.Val107Ala
|
|
NR_130712.2:n.489+337T>C
|
|
|