ENST00000313468.10:c.372+51G>A
MANE Select
|
ENSP00000315774.5:n.372+51G>A
|
|
ENST00000313468.9:c.372+51G>A
|
ENSP00000315774.5:n.372+51G>A
|
|
ENST00000432321.6:n.540G>A
|
|
|
ENST00000524810.5:c.143+51G>A
|
|
|
ENST00000525419.5:c.318+51G>A
|
ENSP00000433521.1:n.318+51G>A
|
|
ENST00000526339.5:c.372+51G>A
|
ENSP00000436287.1:n.372+51G>A
|
|
ENST00000526446.5:c.*427+51G>A
|
ENSP00000433645.1:n.*427+51G>A
|
|
ENST00000528492.1:c.-67+2601G>A
|
ENSP00000432848.1:n.-67+2601G>A
|
|
ENST00000529645.1:c.550+51G>A
|
ENSP00000431293.1:n.550+51G>A
|
|
ENST00000532399.1:n.1128G>A
|
|
|
NM_002496.3:c.372+51G>A
|
NP_002487.1:n.372+51G>A
|
|
XM_005274013.1:c.372+51G>A
|
XP_005274070.1:n.372+51G>A
|
|
XM_005274014.1:c.372+51G>A
|
XP_005274071.1:n.372+51G>A
|
|
XM_005274015.1:c.252+51G>A
|
XP_005274072.1:n.252+51G>A
|
|
XM_011545053.1:c.372+51G>A
|
XP_011543355.1:n.372+51G>A
|
|
NM_002496.4:c.372+51G>A
MANE Select
|
NP_002487.1:n.372+51G>A
|
|