ENST00000314742.13:c.1131A>C
MANE Select
|
ENSP00000318423.8:p.Pro377=
|
|
ENST00000314742.12:c.1131A>C
|
ENSP00000318423.8:p.Pro377=
|
|
ENST00000559149.5:n.1288A>C
|
|
|
ENST00000560133.5:c.774A>C
|
ENSP00000454929.1:p.Pro258=
|
|
ENST00000560783.1:c.100A>C
|
|
|
ENST00000561308.5:c.1131A>C
|
ENSP00000454200.1:p.Pro377=
|
|
NM_001040616.2:c.1131A>C
|
NP_001035706.1:p.Pro377=
|
|
XM_005254941.1:c.1131A>C
|
XP_005254998.1:p.Pro377=
|
|
XM_005254943.1:c.1131A>C
|
XP_005255000.1:p.Pro377=
|
|
XR_243210.2:n.1234A>C
|
|
|
XR_429464.2:n.1234A>C
|
|
|
XR_931862.1:n.1234A>C
|
|
|
XR_931863.1:n.1234A>C
|
|
|
XR_931864.1:n.1234A>C
|
|
|
NM_001352507.1:c.384A>C
|
NP_001339436.1:p.Pro128=
|
|
NM_001352508.1:c.1086A>C
|
NP_001339437.1:p.Pro362=
|
|
NR_148017.1:n.1354A>C
|
|
|
NR_148018.1:n.1354A>C
|
|
|
NR_148019.1:n.1358A>C
|
|
|
XM_005254941.2:c.1131A>C
|
XP_005254998.1:p.Pro377=
|
|
XM_005254943.2:c.1131A>C
|
XP_005255000.1:p.Pro377=
|
|
XM_017022399.2:c.384A>C
|
XP_016877888.1:p.Pro128=
|
|
XM_017022400.2:c.384A>C
|
XP_016877889.1:p.Pro128=
|
|
XM_024449979.1:c.1131A>C
|
XP_024305747.1:p.Pro377=
|
|
XM_024449980.1:c.1131A>C
|
XP_024305748.1:p.Pro377=
|
|
XR_001751346.2:n.2146A>C
|
|
|
XR_001751347.2:n.2146A>C
|
|
|
XR_001751348.2:n.2146A>C
|
|
|
XR_002957655.1:n.2146A>C
|
|
|
XR_931862.3:n.2146A>C
|
|
|
NM_001040616.3:c.1131A>C
MANE Select
|
NP_001035706.2:p.Pro377=
|
|
NM_001352507.2:c.384A>C
|
NP_001339436.1:p.Pro128=
|
|
NM_001352508.2:c.1086A>C
|
NP_001339437.1:p.Pro362=
|
|
NR_148017.2:n.1298A>C
|
|
|
NR_148018.2:n.1298A>C
|
|
|
NR_148019.2:n.1302A>C
|
|
|