ENST00000388996.10:c.778-137A>G
MANE Select
|
ENSP00000373648.3:n.778-137A>G
|
|
ENST00000521134.6:c.418-137A>G
|
ENSP00000429799.1:n.418-137A>G
|
|
ENST00000638588.1:c.451-137A>G
|
ENSP00000491940.1:n.451-137A>G
|
|
ENST00000639358.1:c.428-137A>G
|
|
|
ENST00000639496.1:c.451-137A>G
|
ENSP00000491165.1:n.451-137A>G
|
|
ENST00000388996.8:c.778-137A>G
|
ENSP00000373648.3:n.778-137A>G
|
|
ENST00000519445.5:c.778-137A>G
|
ENSP00000428790.1:n.778-137A>G
|
|
ENST00000519589.1:n.556-137A>G
|
|
|
ENST00000521134.5:c.418-137A>G
|
ENSP00000429799.1:n.418-137A>G
|
|
ENST00000621976.1:c.415-137A>G
|
ENSP00000482510.1:n.415-137A>G
|
|
NM_001204824.1:c.418-137A>G
|
NP_001191753.1:n.418-137A>G
|
|
NM_004519.3:c.778-137A>G
|
NP_004510.1:n.778-137A>G
|
|
XM_005250914.2:c.-379-137A>G
|
XP_005250971.1:n.-379-137A>G
|
|
XM_006716555.2:c.70-137A>G
|
XP_006716618.1:n.70-137A>G
|
|
XM_011517026.1:c.418-137A>G
|
XP_011515328.1:n.418-137A>G
|
|
XM_005250914.3:c.-379-137A>G
|
XP_005250971.1:n.-379-137A>G
|
|
XM_006716555.3:c.70-137A>G
|
XP_006716618.1:n.70-137A>G
|
|
XM_011517026.2:c.418-137A>G
|
XP_011515328.1:n.418-137A>G
|
|
XM_017013400.1:c.556-137A>G
|
XP_016868889.1:n.556-137A>G
|
|
NM_004519.4:c.778-137A>G
MANE Select
|
NP_004510.1:n.778-137A>G
|
|
NM_001204824.2:c.418-137A>G
|
NP_001191753.1:n.418-137A>G
|
|