ENST00000261292.9:c.1377-108C>T
MANE Select
|
ENSP00000261292.4:n.1377-108C>T
|
|
ENST00000261292.8:c.1377-108C>T
|
ENSP00000261292.4:n.1377-108C>T
|
|
ENST00000427224.6:c.1155-108C>T
|
ENSP00000387978.2:n.1155-108C>T
|
|
NM_001308006.1:c.1155-108C>T
|
NP_001294935.1:n.1155-108C>T
|
|
NM_006033.2:c.1377-108C>T
|
NP_006024.1:n.1377-108C>T
|
|
NM_006033.3:c.1377-108C>T
|
NP_006024.1:n.1377-108C>T
|
|
XM_005258390.1:c.1485-108C>T
|
XP_005258447.1:n.1485-108C>T
|
|
XM_011526265.1:c.1263-108C>T
|
XP_011524567.1:n.1263-108C>T
|
|
XM_011526267.1:c.1137-108C>T
|
XP_011524569.1:n.1137-108C>T
|
|
XM_011526265.3:c.1263-108C>T
|
XP_011524567.1:n.1263-108C>T
|
|
XM_017026095.1:c.786-108C>T
|
XP_016881584.1:n.786-108C>T
|
|
NM_006033.4:c.1377-108C>T
MANE Select
|
NP_006024.1:n.1377-108C>T
|
|
NM_001308006.2:c.1155-108C>T
|
NP_001294935.1:n.1155-108C>T
|
|