ENST00000369458.8:c.822T>G
MANE Select
|
ENSP00000358470.3:p.Pro274=
|
|
ENST00000328189.7:c.474T>G
|
ENSP00000328168.3:p.Pro158=
|
|
ENST00000359008.8:c.831T>G
|
ENSP00000351899.4:p.Pro277=
|
|
ENST00000369458.7:c.822T>G
|
ENSP00000358470.3:p.Pro274=
|
|
ENST00000539893.5:c.537T>G
|
ENSP00000444724.1:p.Pro179=
|
|
NM_001253849.1:c.537T>G
|
NP_001240778.1:p.Pro179=
|
|
NM_001253850.1:c.474T>G
|
NP_001240779.1:p.Pro158=
|
|
NM_024626.3:c.822T>G
|
NP_078902.2:p.Pro274=
|
|
NR_045603.1:n.1017T>G
|
|
|
NR_045604.1:n.721T>G
|
|
|
XM_011542143.1:c.873T>G
|
XP_011540445.1:p.Pro291=
|
|
XM_011542144.1:c.876T>G
|
XP_011540446.1:p.Pro292=
|
|
XM_011542145.1:c.837T>G
|
XP_011540447.1:p.Pro279=
|
|
XM_011542143.2:c.972T>G
|
XP_011540445.2:p.Pro324=
|
|
XM_017002335.2:c.837T>G
|
XP_016857824.1:p.Pro279=
|
|
NM_024626.4:c.822T>G
MANE Select
|
NP_078902.2:p.Pro274=
|
|
NR_045603.2:n.984T>G
|
|
|
NR_045604.2:n.688T>G
|
|
|
NM_001253849.2:c.537T>G
|
NP_001240778.1:p.Pro179=
|
|
NM_001253850.2:c.474T>G
|
NP_001240779.1:p.Pro158=
|
|