ENST00000650793.2:n.587G>C
|
|
|
ENST00000697612.1:n.1264+1G>C
|
|
|
ENST00000374881.3:c.395+1G>C
|
ENSP00000364015.2:n.395+1G>C
|
|
ENST00000374882.8:c.407+1G>C
MANE Select
|
ENSP00000364016.4:n.407+1G>C
|
|
ENST00000650411.1:n.1728+1G>C
|
|
|
ENST00000650793.1:n.587G>C
|
|
|
ENST00000374881.2:c.395+1G>C
|
ENSP00000364015.2:n.395+1G>C
|
|
ENST00000374882.7:c.407+1G>C
|
ENSP00000364016.3:n.407+1G>C
|
|
ENST00000395339.7:c.335+1G>C
|
ENSP00000378748.3:n.335+1G>C
|
|
ENST00000484003.1:n.791+1G>C
|
|
|
NM_004159.4:c.395+1G>C
|
NP_004150.1:n.395+1G>C
|
|
NM_148919.3:c.407+1G>C
|
NP_683720.2:n.407+1G>C
|
|
NM_148919.4:c.407+1G>C
MANE Select
|
NP_683720.2:n.407+1G>C
|
|
NM_004159.5:c.395+1G>C
|
NP_004150.1:n.395+1G>C
|
|