ENST00000622443.3:c.784-387T>G
|
ENSP00000482268.2:n.784-387T>G
|
|
ENST00000532059.6:c.787-387T>G
MANE Select
|
ENSP00000435712.1:n.787-387T>G
|
|
ENST00000335135.8:c.784-387T>G
|
ENSP00000334458.4:n.784-387T>G
|
|
ENST00000526716.5:c.166-387T>G
|
ENSP00000435347.1:n.166-387T>G
|
|
ENST00000528712.5:c.166-387T>G
|
ENSP00000435043.1:n.166-387T>G
|
|
ENST00000532059.5:c.787-387T>G
|
ENSP00000435712.1:n.787-387T>G
|
|
ENST00000622443.2:c.781-387T>G
|
ENSP00000482268.1:n.781-387T>G
|
|
NM_001308093.1:c.787-387T>G
|
NP_001295022.1:n.787-387T>G
|
|
NM_001308094.1:c.166-387T>G
|
NP_001295023.1:n.166-387T>G
|
|
NM_002052.3:c.784-387T>G
|
NP_002043.2:n.784-387T>G
|
|
NM_002052.4:c.784-387T>G
|
NP_002043.2:n.784-387T>G
|
|
XM_005272385.3:c.787-387T>G
|
XP_005272442.1:n.787-387T>G
|
|
XM_005272386.1:c.787-387T>G
|
XP_005272443.1:n.787-387T>G
|
|
XM_006716248.1:c.787-387T>G
|
XP_006716311.1:n.787-387T>G
|
|
XM_011543817.1:c.787-387T>G
|
XP_011542119.1:n.787-387T>G
|
|
XM_011543818.1:c.787-387T>G
|
XP_011542120.1:n.787-387T>G
|
|
XM_005272385.4:c.787-387T>G
|
XP_005272442.1:n.787-387T>G
|
|
XM_011543817.3:c.787-387T>G
|
XP_011542119.1:n.787-387T>G
|
|
XM_011543818.2:c.787-387T>G
|
XP_011542120.1:n.787-387T>G
|
|
XM_017013312.2:c.787-387T>G
|
XP_016868801.1:n.787-387T>G
|
|
NM_001308093.3:c.787-387T>G
MANE Select
|
NP_001295022.1:n.787-387T>G
|
|
NM_001308094.2:c.166-387T>G
|
NP_001295023.1:n.166-387T>G
|
|
NM_001374273.1:c.166-387T>G
|
NP_001361202.1:n.166-387T>G
|
|
NM_001374274.1:c.165+639T>G
|
NP_001361203.1:n.165+639T>G
|
|
NM_002052.5:c.784-387T>G
|
NP_002043.2:n.784-387T>G
|
|