ENST00000382061.5:c.1232T>C
|
ENSP00000371493.4:p.Val411Ala
|
|
ENST00000453066.6:c.1232T>C
MANE Select
|
ENSP00000402286.2:p.Val411Ala
|
|
ENST00000324015.7:c.1232T>C
|
ENSP00000321853.3:p.Val411Ala
|
|
ENST00000382061.4:c.1232T>C
|
ENSP00000371493.4:p.Val411Ala
|
|
ENST00000450523.6:c.1040T>C
|
ENSP00000403877.2:p.Val347Ala
|
|
NM_000934.3:c.1232T>C , LRG_885t1:c.1232T>C
|
NP_000925.2:p.Val411Ala
|
|
NM_001165920.1:c.1232T>C
|
NP_001159392.1:p.Val411Ala
|
|
NM_001165921.1:c.1040T>C
|
NP_001159393.1:p.Val347Ala
|
|
XM_005256699.3:c.1337T>C
|
XP_005256756.1:p.Val446Ala
|
|
XM_005256700.3:c.1244T>C
|
XP_005256757.1:p.Val415Ala
|
|
XM_005256701.3:c.1280T>C
|
XP_005256758.2:p.Val427Ala
|
|
XM_005256703.3:c.1151T>C
|
XP_005256760.1:p.Val384Ala
|
|
XM_005256701.4:c.1280T>C
|
XP_005256758.2:p.Val427Ala
|
|
XM_017024765.1:c.1244T>C
|
XP_016880254.1:p.Val415Ala
|
|
XM_024450805.1:c.1244T>C
|
XP_024306573.1:p.Val415Ala
|
|
NM_000934.4:c.1232T>C
MANE Select
|
NP_000925.2:p.Val411Ala
|
|
NM_001165921.2:c.1040T>C
|
NP_001159393.1:p.Val347Ala
|
|