ENST00000389857.11:c.2736+199C>A
MANE Select
|
ENSP00000374507.6:n.2736+199C>A
|
|
ENST00000389857.10:c.2736+199C>A
|
ENSP00000374507.6:n.2736+199C>A
|
|
NM_001080414.3:c.2736+199C>A
|
NP_001073883.2:n.2736+199C>A
|
|
XM_005267691.3:c.2736+199C>A
|
XP_005267748.1:n.2736+199C>A
|
|
XM_011536796.1:c.2628+199C>A
|
XP_011535098.1:n.2628+199C>A
|
|
XR_429316.2:n.2864+199C>A
|
|
|
XR_943459.1:n.2864+199C>A
|
|
|
XM_005267691.5:c.2736+199C>A
|
XP_005267748.1:n.2736+199C>A
|
|
XM_011536796.2:c.2628+199C>A
|
XP_011535098.1:n.2628+199C>A
|
|
XM_017021335.2:c.2736+199C>A
|
XP_016876824.1:n.2736+199C>A
|
|
XM_017021336.1:c.-56+199C>A
|
XP_016876825.1:n.-56+199C>A
|
|
XM_017021337.2:c.2736+199C>A
|
XP_016876826.1:n.2736+199C>A
|
|
XR_429316.4:n.2862+199C>A
|
|
|
NM_001080414.4:c.2736+199C>A
MANE Select
|
NP_001073883.2:n.2736+199C>A
|
|