ENST00000295897.9:c.714-1G>C
MANE Select
|
ENSP00000295897.4:n.714-1G>C
|
|
ENST00000295897.8:c.714-1G>C
|
ENSP00000295897.4:n.714-1G>C
|
|
ENST00000401494.7:c.369-1G>C
|
ENSP00000384695.3:n.369-1G>C
|
|
ENST00000415165.6:c.138-1G>C
|
ENSP00000401820.2:n.138-1G>C
|
|
ENST00000476441.6:c.311-1G>C
|
ENSP00000423727.1:n.311-1G>C
|
|
ENST00000503124.5:c.264-1G>C
|
ENSP00000421027.1:n.264-1G>C
|
|
ENST00000505649.5:n.400-1G>C
|
|
|
ENST00000507673.1:n.31-1G>C
|
|
|
ENST00000509063.5:c.714-1G>C
|
ENSP00000422784.1:n.714-1G>C
|
|
ENST00000511370.1:c.247-1G>C
|
|
|
ENST00000621085.4:c.490+2633G>C
|
ENSP00000483421.1:n.490+2633G>C
|
|
ENST00000621628.4:c.486+2919G>C
|
ENSP00000480485.1:n.486+2919G>C
|
|
NM_000477.5:c.714-1G>C
|
NP_000468.1:n.714-1G>C
|
|
NM_000477.6:c.714-1G>C
|
NP_000468.1:n.714-1G>C
|
|
NM_000477.7:c.714-1G>C
MANE Select
|
NP_000468.1:n.714-1G>C
|
|