ENST00000367574.9:c.137-314A>G
|
ENSP00000356546.6:n.137-314A>G
|
|
ENST00000537758.6:c.137-314A>G
|
ENSP00000446401.3:n.137-314A>G
|
|
ENST00000682661.1:n.296-314A>G
|
|
|
ENST00000683923.1:c.137-314A>G
|
ENSP00000506737.1:n.137-314A>G
|
|
ENST00000684722.1:n.319-314A>G
|
|
|
ENST00000326194.11:c.137-314A>G
MANE Select
|
ENSP00000322304.6:n.137-314A>G
|
|
ENST00000485288.7:c.137-385A>G
|
ENSP00000420445.3:n.137-385A>G
|
|
ENST00000326194.10:c.137-314A>G
|
ENSP00000322304.6:n.137-314A>G
|
|
ENST00000355961.8:c.137-314A>G
|
ENSP00000348233.4:n.137-314A>G
|
|
ENST00000359882.8:c.137-314A>G
|
ENSP00000352946.4:n.137-314A>G
|
|
ENST00000361988.7:c.137-314A>G
|
ENSP00000354978.3:n.137-314A>G
|
|
ENST00000367574.8:c.137-314A>G
|
ENSP00000356546.5:n.137-314A>G
|
|
ENST00000470275.2:c.137-385A>G
|
ENSP00000418644.2:n.137-385A>G
|
|
ENST00000472520.5:c.137-911A>G
|
ENSP00000419858.1:n.137-911A>G
|
|
ENST00000485288.6:c.329-385A>G
|
ENSP00000420445.2:n.329-385A>G
|
|
ENST00000486272.1:n.487-314A>G
|
|
|
ENST00000489940.5:c.137-314A>G
|
ENSP00000419212.1:n.137-314A>G
|
|
ENST00000491243.5:n.247-385A>G
|
|
|
ENST00000528612.5:c.137-385A>G
|
ENSP00000431224.1:n.137-385A>G
|
|
ENST00000537758.5:c.137-314A>G
|
ENSP00000446401.2:n.137-314A>G
|
|
NM_001282167.1:c.-6-385A>G
|
NP_001269096.1:n.-6-385A>G
|
|
NM_022825.3:c.137-314A>G
|
NP_073736.2:n.137-314A>G
|
|
NM_203473.2:c.137-314A>G
|
NP_982299.1:n.137-314A>G
|
|
NM_203474.1:c.137-314A>G
|
NP_982300.1:n.137-314A>G
|
|
NM_203475.2:c.137-314A>G
|
NP_982301.1:n.137-314A>G
|
|
XM_005272635.1:c.476-314A>G
|
XP_005272692.1:n.476-314A>G
|
|
XM_005272636.1:c.476-314A>G
|
XP_005272693.1:n.476-314A>G
|
|
XM_005272637.1:c.389-314A>G
|
XP_005272694.1:n.389-314A>G
|
|
XM_006724544.2:c.242-314A>G
|
XP_006724607.1:n.242-314A>G
|
|
XM_006724545.2:c.259-385A>G
|
XP_006724608.1:n.259-385A>G
|
|
XM_006724546.2:c.137-314A>G
|
XP_006724609.1:n.137-314A>G
|
|
XM_006724547.1:c.-6-385A>G
|
XP_006724610.1:n.-6-385A>G
|
|
XM_011543948.1:c.-6-385A>G
|
XP_011542250.1:n.-6-385A>G
|
|
XM_024452425.1:c.476-314A>G
|
XP_024308193.1:n.476-314A>G
|
|
NM_001282167.2:c.-6-385A>G
|
NP_001269096.1:n.-6-385A>G
|
|
NM_022825.4:c.137-314A>G
|
NP_073736.2:n.137-314A>G
|
|
NM_203473.3:c.137-314A>G
|
NP_982299.1:n.137-314A>G
|
|
NM_203475.3:c.137-314A>G
MANE Select
|
NP_982301.1:n.137-314A>G
|
|