ENST00000583780.2:c.519+2789A>G
|
ENSP00000462041.2:n.519+2789A>G
|
|
ENST00000316694.8:c.519+2789A>G
MANE Select
|
ENSP00000318868.3:n.519+2789A>G
|
|
ENST00000316694.7:c.519+2789A>G
|
ENSP00000318868.3:n.519+2789A>G
|
|
ENST00000352886.10:c.105+2789A>G
|
ENSP00000345881.7:n.105+2789A>G
|
|
ENST00000354098.7:c.519+2789A>G
|
ENSP00000318805.3:n.519+2789A>G
|
|
ENST00000579558.5:n.668+2789A>G
|
|
|
ENST00000580002.5:c.*16+2789A>G
|
ENSP00000462043.1:n.*16+2789A>G
|
|
NM_001281786.1:c.105+2789A>G
|
NP_001268715.1:n.105+2789A>G
|
|
NM_004169.4:c.519+2789A>G
|
NP_004160.3:n.519+2789A>G
|
|
NM_148918.2:c.519+2789A>G
|
NP_683718.1:n.519+2789A>G
|
|
XM_005256767.2:c.519+2789A>G
|
XP_005256824.1:n.519+2789A>G
|
|
XM_011523992.1:c.519+2789A>G
|
XP_011522294.1:n.519+2789A>G
|
|
XM_005256767.3:c.519+2789A>G
|
XP_005256824.1:n.519+2789A>G
|
|
XM_011523992.3:c.519+2789A>G
|
XP_011522294.1:n.519+2789A>G
|
|
XM_017024957.1:c.519+2789A>G
|
XP_016880446.1:n.519+2789A>G
|
|
XM_017024958.1:c.519+2789A>G
|
XP_016880447.1:n.519+2789A>G
|
|
XM_024450887.1:c.519+2789A>G
|
XP_024306655.1:n.519+2789A>G
|
|
XM_024450888.1:c.105+2789A>G
|
XP_024306656.1:n.105+2789A>G
|
|
XM_024450889.1:c.105+2789A>G
|
XP_024306657.1:n.105+2789A>G
|
|
XM_024450890.1:c.105+2789A>G
|
XP_024306658.1:n.105+2789A>G
|
|
NM_004169.5:c.519+2789A>G
MANE Select
|
NP_004160.3:n.519+2789A>G
|
|
NM_001281786.2:c.105+2789A>G
|
NP_001268715.1:n.105+2789A>G
|
|
NM_148918.3:c.519+2789A>G
|
NP_683718.1:n.519+2789A>G
|
|