ENST00000274376.11:c.539+63G>A
MANE Select
|
ENSP00000274376.6:n.539+63G>A
|
|
ENST00000274376.10:c.539+63G>A
|
ENSP00000274376.6:n.539+63G>A
|
|
ENST00000456692.6:c.6G>A
|
ENSP00000411221.2:p.Lys2=
|
|
ENST00000506290.1:c.-8G>A
|
ENSP00000420905.1:n.-8G>A
|
|
ENST00000512763.5:c.-92G>A
|
ENSP00000422008.1:n.-92G>A
|
|
ENST00000515800.6:c.539+63G>A
|
ENSP00000423395.2:n.539+63G>A
|
|
NM_002890.2:c.539+63G>A
|
NP_002881.1:n.539+63G>A
|
|
NM_022650.2:c.6G>A
|
NP_072179.1:p.Lys2=
|
|
XM_011543525.1:c.539+63G>A
|
XP_011541827.1:n.539+63G>A
|
|
XM_011543526.1:c.539+63G>A
|
XP_011541828.1:n.539+63G>A
|
|
XM_011543527.1:c.539+63G>A
|
XP_011541829.1:n.539+63G>A
|
|
XM_011543525.2:c.539+63G>A
|
XP_011541827.1:n.539+63G>A
|
|
XM_011543527.3:c.539+63G>A
|
XP_011541829.1:n.539+63G>A
|
|
NM_002890.3:c.539+63G>A
MANE Select
|
NP_002881.1:n.539+63G>A
|
|
NM_022650.3:c.6G>A
|
NP_072179.1:p.Lys2=
|
|