ENST00000453304.6:c.1108+3763T>C
MANE Select
|
ENSP00000406022.1:n.1108+3763T>C
|
|
ENST00000453304.5:c.1108+3763T>C
|
ENSP00000406022.1:n.1108+3763T>C
|
|
ENST00000506749.5:c.1108+3763T>C
|
ENSP00000426153.1:n.1108+3763T>C
|
|
ENST00000513796.5:c.1108+3763T>C
|
ENSP00000426924.1:n.1108+3763T>C
|
|
ENST00000610318.4:c.985+3763T>C
|
ENSP00000483905.1:n.985+3763T>C
|
|
NM_003728.3:c.1108+3763T>C
|
NP_003719.3:n.1108+3763T>C
|
|
XM_005263321.2:c.1108+3763T>C
|
XP_005263378.1:n.1108+3763T>C
|
|
XM_005263321.3:c.1108+3763T>C
|
XP_005263378.1:n.1108+3763T>C
|
|
XM_017008789.1:c.7+3763T>C
|
XP_016864278.1:n.7+3763T>C
|
|
XM_017008790.1:c.7+3763T>C
|
XP_016864279.1:n.7+3763T>C
|
|
NM_003728.4:c.1108+3763T>C
MANE Select
|
NP_003719.3:n.1108+3763T>C
|
|