ENST00000222812.8:c.30+691A>C
MANE Select
|
ENSP00000222812.3:n.30+691A>C
|
|
ENST00000222812.7:c.30+691A>C
|
ENSP00000222812.3:n.30+691A>C
|
|
ENST00000395154.7:c.30+691A>C
|
ENSP00000378583.3:n.30+691A>C
|
|
ENST00000395155.3:c.30+691A>C
|
ENSP00000378584.3:n.30+691A>C
|
|
ENST00000395156.7:c.30+691A>C
|
ENSP00000378585.3:n.30+691A>C
|
|
ENST00000462135.1:n.71+691A>C
|
|
|
ENST00000470878.5:n.25+691A>C
|
|
|
NM_001165903.1:c.30+691A>C
|
NP_001159375.1:n.30+691A>C
|
|
NM_004603.3:c.30+691A>C
|
NP_004594.1:n.30+691A>C
|
|
XR_242263.1:n.101+691A>C
|
|
|
XR_927527.1:n.101+691A>C
|
|
|
XM_017012567.2:c.30+691A>C
|
XP_016868056.1:n.30+691A>C
|
|
XR_242263.2:n.72+691A>C
|
|
|
XR_927527.2:n.72+691A>C
|
|
|
NM_004603.4:c.30+691A>C
MANE Select
|
NP_004594.1:n.30+691A>C
|
|
NM_001165903.2:c.30+691A>C
|
NP_001159375.1:n.30+691A>C
|
|