ENST00000374866.9:c.2130+147T>C
MANE Select
|
ENSP00000364000.3:n.2130+147T>C
|
|
ENST00000374866.7:c.2130+147T>C
|
ENSP00000364000.3:n.2130+147T>C
|
|
ENST00000470524.2:n.236+147T>C
|
|
|
ENST00000618828.1:c.969+147T>C
|
ENSP00000482184.1:n.969+147T>C
|
|
NM_000393.3:c.2130+147T>C
|
NP_000384.2:n.2130+147T>C
|
|
XM_011510573.1:c.1992+147T>C
|
XP_011508875.1:n.1992+147T>C
|
|
NM_000393.4:c.2130+147T>C
|
NP_000384.2:n.2130+147T>C
|
|
XM_011510573.3:c.1992+147T>C
|
XP_011508875.1:n.1992+147T>C
|
|
NM_000393.5:c.2130+147T>C
MANE Select
|
NP_000384.2:n.2130+147T>C
|
|