ENST00000621198.5:c.1613+356A>T
MANE Select
|
ENSP00000480050.1:n.1613+356A>T
|
|
ENST00000439861.5:n.1232+356A>T
|
|
|
ENST00000621198.4:c.1613+356A>T
|
ENSP00000480050.1:n.1613+356A>T
|
|
NM_133625.4:c.1613+356A>T
|
NP_598328.1:n.1613+356A>T
|
|
XM_006713312.2:c.1130+356A>T
|
XP_006713375.1:n.1130+356A>T
|
|
XM_006713313.2:c.842+356A>T
|
XP_006713376.1:n.842+356A>T
|
|
XM_006713312.4:c.1130+356A>T
|
XP_006713375.1:n.1130+356A>T
|
|
XM_017007087.1:c.941+356A>T
|
XP_016862576.1:n.941+356A>T
|
|
NM_133625.5:c.1613+356A>T
|
NP_598328.1:n.1613+356A>T
|
|
NM_133625.6:c.1613+356A>T
MANE Select
|
NP_598328.1:n.1613+356A>T
|
|