ENST00000263080.3:c.384T>G
(ASPA)
MANE Select
|
ENSP00000263080.2:p.Leu128=
|
|
ENST00000263080.2:c.384T>G
(ASPA)
|
ENSP00000263080.2:p.Leu128=
|
|
ENST00000456349.6:c.384T>G
(ASPA)
|
ENSP00000409976.2:p.Leu128=
|
|
ENST00000541913.5:c.-73-12352A>C
(SPATA22)
|
ENSP00000441920.1:n.-73-12352A>C
|
|
ENST00000570318.1:c.-73-12352A>C
(SPATA22)
|
ENSP00000459147.1:n.-73-12352A>C
|
|
ENST00000571278.1:c.*118T>G
(ASPA)
|
ENSP00000461358.1:n.*118T>G
|
|
NM_000049.2:c.384T>G
(ASPA)
|
NP_000040.1:p.Leu128=
|
|
NM_001128085.1:c.384T>G
(ASPA)
|
NP_001121557.1:p.Leu128=
|
|
XM_005256829.1:c.-73-12352A>C
(SPATA22)
|
XP_005256886.1:n.-73-12352A>C
|
|
XM_005256830.1:c.-73-12352A>C
(SPATA22)
|
XP_005256887.1:n.-73-12352A>C
|
|
XM_006721527.2:c.384T>G
(ASPA)
|
XP_006721590.1:p.Leu128=
|
|
XR_934026.1:n.559T>G
(ASPA)
|
|
|
NM_001321336.1:c.-73-12352A>C
(SPATA22)
|
NP_001308265.1:n.-73-12352A>C
|
|
NM_001321337.1:c.-73-12352A>C
(SPATA22)
|
NP_001308266.1:n.-73-12352A>C
|
|
XM_017024661.1:c.384T>G
(ASPA)
|
XP_016880150.1:p.Leu128=
|
|
XM_024450764.1:c.384T>G
(ASPA)
|
XP_024306532.1:p.Leu128=
|
|
XR_934026.2:n.559T>G
(ASPA)
|
|
|
NM_000049.3:c.384T>G
(ASPA)
|
NP_000040.1:p.Leu128=
|
|
NM_000049.4:c.384T>G
(ASPA)
MANE Select
|
NP_000040.1:p.Leu128=
|
|
NM_001321336.2:c.-73-12352A>C
(SPATA22)
|
NP_001308265.1:n.-73-12352A>C
|
|
NM_001321337.2:c.-73-12352A>C
(SPATA22)
|
NP_001308266.1:n.-73-12352A>C
|
|