ENST00000395544.9:c.1809+1G>C
MANE Select
|
ENSP00000378914.4:n.1809+1G>C
|
|
ENST00000361658.6:c.1809+1G>C
|
ENSP00000354877.2:n.1809+1G>C
|
|
ENST00000395544.8:c.1809+1G>C
|
ENSP00000378914.4:n.1809+1G>C
|
|
NM_001142610.1:c.1809+1G>C
|
NP_001136082.1:n.1809+1G>C
|
|
NM_014683.3:c.1809+1G>C
|
NP_055498.3:n.1809+1G>C
|
|
XM_011524087.1:c.1455+1G>C
|
XP_011522389.1:n.1455+1G>C
|
|
XR_934124.1:n.2143+1G>C
|
|
|
XR_934125.1:n.2143+1G>C
|
|
|
XM_011524087.2:c.1455+1G>C
|
XP_011522389.1:n.1455+1G>C
|
|
XM_017025424.2:c.1872+1G>C
|
XP_016880913.1:n.1872+1G>C
|
|
XM_017025425.2:c.1872+1G>C
|
XP_016880914.1:n.1872+1G>C
|
|
XM_017025426.2:c.1872+1G>C
|
XP_016880915.1:n.1872+1G>C
|
|
XM_017025427.2:c.1032+1G>C
|
XP_016880916.1:n.1032+1G>C
|
|
XM_017025428.2:c.1032+1G>C
|
XP_016880917.1:n.1032+1G>C
|
|
XR_001752700.2:n.2352+1G>C
|
|
|
XR_001752701.2:n.2352+1G>C
|
|
|
NM_014683.4:c.1809+1G>C
MANE Select
|
NP_055498.3:n.1809+1G>C
|
|
NM_001142610.2:c.1809+1G>C
|
NP_001136082.1:n.1809+1G>C
|
|