ENST00000374479.4:c.1160+17G>C
MANE Select
|
ENSP00000363603.3:n.1160+17G>C
|
|
ENST00000374479.3:c.1160+17G>C
|
ENSP00000363603.3:n.1160+17G>C
|
|
NM_000147.4:c.1160+17G>C
|
NP_000138.2:n.1160+17G>C
|
|
XM_005245821.1:c.785+17G>C
|
XP_005245878.1:n.785+17G>C
|
|
XM_011541167.1:c.527+17G>C
|
XP_011539469.1:n.527+17G>C
|
|
XM_005245821.3:c.785+17G>C
|
XP_005245878.1:n.785+17G>C
|
|
XM_011541167.3:c.527+17G>C
|
XP_011539469.1:n.527+17G>C
|
|
XM_017000905.2:c.857+17G>C
|
XP_016856394.1:n.857+17G>C
|
|
NM_000147.5:c.1160+17G>C
MANE Select
|
NP_000138.2:n.1160+17G>C
|
|
NR_174379.1:n.1338+17G>C
|
|
|
NR_174380.1:n.1387+17G>C
|
|
|
NR_174381.1:n.1226+17G>C
|
|
|
NR_174382.1:n.1623+17G>C
|
|
|