|
ENST00000355773.6:c.1259+2T>C
MANE Select
|
ENSP00000348019.5:n.1259+2T>C
|
|
|
ENST00000355773.5:c.1259+2T>C
|
ENSP00000348019.5:n.1259+2T>C
|
|
|
NM_012434.4:c.1259+2T>C
|
NP_036566.1:n.1259+2T>C
|
|
|
XM_005248710.2:c.1208+2T>C
|
XP_005248767.1:n.1208+2T>C
|
|
|
XM_005248711.1:c.1061+2T>C
|
XP_005248768.1:n.1061+2T>C
|
|
|
XM_011535750.1:c.1111+4917T>C
|
XP_011534052.1:n.1111+4917T>C
|
|
|
NM_012434.5:c.1259+2T>C
MANE Select
|
NP_036566.1:n.1259+2T>C
|
|
|
NM_001382629.1:c.1028+2T>C
|
NP_001369558.1:n.1028+2T>C
|
|
|
NM_001382630.1:c.1259+2T>C
|
NP_001369559.1:n.1259+2T>C
|
|
|
NM_001382631.1:c.1280+2T>C
|
NP_001369560.1:n.1280+2T>C
|
|
|
NM_001382632.1:c.1172+2T>C
|
NP_001369561.1:n.1172+2T>C
|
|
|
NM_001382633.1:c.1259+2T>C
|
NP_001369562.1:n.1259+2T>C
|
|
|
NM_001382634.1:c.1100+2T>C
|
NP_001369563.1:n.1100+2T>C
|
|
|
NM_001382635.1:c.1256+2T>C
|
NP_001369564.1:n.1256+2T>C
|
|
|
NM_001382636.1:c.941+2T>C
|
NP_001369565.1:n.941+2T>C
|
|
