ENST00000369244.7:c.1702+316A>G
MANE Select
|
ENSP00000358247.1:n.1702+316A>G
|
|
ENST00000229971.2:c.1702+316A>G
|
ENSP00000229971.1:n.1702+316A>G
|
|
ENST00000369244.6:c.1702+316A>G
|
ENSP00000358247.1:n.1702+316A>G
|
|
NM_001278716.1:c.1702+316A>G
|
NP_001265645.1:n.1702+316A>G
|
|
NM_012160.4:c.1702+316A>G
|
NP_036292.2:n.1702+316A>G
|
|
NR_103836.1:n.1747+316A>G
|
|
|
XM_005266930.1:c.1630+316A>G
|
XP_005266987.1:n.1630+316A>G
|
|
XM_005266930.3:c.1630+316A>G
|
XP_005266987.1:n.1630+316A>G
|
|
XM_017010726.1:c.1702+316A>G
|
XP_016866215.1:n.1702+316A>G
|
|
XM_017010727.2:c.1630+316A>G
|
XP_016866216.1:n.1630+316A>G
|
|
XM_017010728.1:c.976+316A>G
|
XP_016866217.1:n.976+316A>G
|
|
NM_001278716.2:c.1702+316A>G
MANE Select
|
NP_001265645.1:n.1702+316A>G
|
|
NR_103836.2:n.1687+316A>G
|
|
|
NM_012160.5:c.1702+316A>G
|
NP_036292.2:n.1702+316A>G
|
|