ENST00000262493.12:c.724-139G>C
MANE Select
|
ENSP00000262493.6:n.724-139G>C
|
|
ENST00000562316.6:c.391-139G>C
|
ENSP00000457238.2:n.391-139G>C
|
|
ENST00000564727.2:c.28-139G>C
|
ENSP00000454971.2:n.28-139G>C
|
|
ENST00000568375.2:c.116-3621G>C
|
|
|
ENST00000638185.1:n.939-139G>C
|
|
|
ENST00000638210.1:n.1024-139G>C
|
|
|
ENST00000638705.1:c.724-139G>C
|
ENSP00000491223.1:n.724-139G>C
|
|
ENST00000638836.1:n.634-139G>C
|
|
|
ENST00000639055.1:n.1445-139G>C
|
|
|
ENST00000639251.1:n.625-139G>C
|
|
|
ENST00000639268.1:c.359-139G>C
|
|
|
ENST00000639341.1:c.249-139G>C
|
|
|
ENST00000639770.1:c.762-139G>C
|
ENSP00000491999.1:n.762-139G>C
|
|
ENST00000640390.1:n.654-139G>C
|
|
|
ENST00000640469.1:c.88-139G>C
|
ENSP00000491875.1:n.88-139G>C
|
|
ENST00000640560.1:n.500-139G>C
|
|
|
ENST00000640893.1:c.*122-139G>C
|
ENSP00000492677.1:n.*122-139G>C
|
|
ENST00000262493.10:c.724-139G>C
|
ENSP00000262493.6:n.724-139G>C
|
|
ENST00000568375.1:n.116-3621G>C
|
|
|
NM_020988.2:c.724-139G>C
|
NP_066268.1:n.724-139G>C
|
|
XM_011523003.1:c.598-139G>C
|
XP_011521305.1:n.598-139G>C
|
|
XM_011523003.3:c.598-139G>C
|
XP_011521305.1:n.598-139G>C
|
|
NM_020988.3:c.724-139G>C
MANE Select
|
NP_066268.1:n.724-139G>C
|
|