ENST00000263080.3:c.744+338A>T
(ASPA)
MANE Select
|
ENSP00000263080.2:n.744+338A>T
|
|
ENST00000263080.2:c.744+338A>T
(ASPA)
|
ENSP00000263080.2:n.744+338A>T
|
|
ENST00000456349.6:c.744+338A>T
(ASPA)
|
ENSP00000409976.2:n.744+338A>T
|
|
ENST00000541913.5:c.-74+18615T>A
(SPATA22)
|
ENSP00000441920.1:n.-74+18615T>A
|
|
ENST00000570318.1:c.-74+18814T>A
(SPATA22)
|
ENSP00000459147.1:n.-74+18814T>A
|
|
NM_000049.2:c.744+338A>T
(ASPA)
|
NP_000040.1:n.744+338A>T
|
|
NM_001128085.1:c.744+338A>T
(ASPA)
|
NP_001121557.1:n.744+338A>T
|
|
XM_005256829.1:c.-74+18615T>A
(SPATA22)
|
XP_005256886.1:n.-74+18615T>A
|
|
XM_005256830.1:c.-74+18615T>A
(SPATA22)
|
XP_005256887.1:n.-74+18615T>A
|
|
XM_006721527.2:c.744+338A>T
(ASPA)
|
XP_006721590.1:n.744+338A>T
|
|
XR_934026.1:n.919+338A>T
(ASPA)
|
|
|
NM_001321336.1:c.-74+18615T>A
(SPATA22)
|
NP_001308265.1:n.-74+18615T>A
|
|
NM_001321337.1:c.-74+18615T>A
(SPATA22)
|
NP_001308266.1:n.-74+18615T>A
|
|
XM_017024661.1:c.744+338A>T
(ASPA)
|
XP_016880150.1:n.744+338A>T
|
|
XM_024450764.1:c.744+338A>T
(ASPA)
|
XP_024306532.1:n.744+338A>T
|
|
XR_934026.2:n.919+338A>T
(ASPA)
|
|
|
NM_000049.3:c.744+338A>T
(ASPA)
|
NP_000040.1:n.744+338A>T
|
|
NM_000049.4:c.744+338A>T
(ASPA)
MANE Select
|
NP_000040.1:n.744+338A>T
|
|
NM_001321336.2:c.-74+18615T>A
(SPATA22)
|
NP_001308265.1:n.-74+18615T>A
|
|
NM_001321337.2:c.-74+18615T>A
(SPATA22)
|
NP_001308266.1:n.-74+18615T>A
|
|