ENST00000294066.7:c.2412A>C
MANE Select
|
ENSP00000294066.2:p.Pro804=
|
|
ENST00000294066.6:c.2412A>C
|
ENSP00000294066.2:p.Pro804=
|
|
ENST00000377350.7:c.2388A>C
|
ENSP00000366567.3:p.Pro796=
|
|
ENST00000424945.5:c.724A>C
|
|
|
ENST00000433890.5:c.2359A>C
|
ENSP00000413167.1:n.2359A>C
|
|
ENST00000435926.5:c.*2212A>C
|
ENSP00000400594.1:n.*2212A>C
|
|
ENST00000470088.5:n.1354A>C
|
|
|
NM_001307990.1:c.2388A>C
|
NP_001294919.1:p.Pro796=
|
|
NM_004579.3:c.2412A>C
|
NP_004570.2:p.Pro804=
|
|
NM_004579.4:c.2412A>C
|
NP_004570.2:p.Pro804=
|
|
XM_011545202.1:c.2388A>C
|
XP_011543504.1:p.Pro796=
|
|
XM_011545203.1:c.2343A>C
|
XP_011543505.1:p.Pro781=
|
|
XM_011545204.1:c.2280A>C
|
XP_011543506.1:p.Pro760=
|
|
XM_011545204.3:c.2280A>C
|
XP_011543506.1:p.Pro760=
|
|
XM_017018093.2:c.2256A>C
|
XP_016873582.1:p.Pro752=
|
|
XM_017018095.2:c.1812A>C
|
XP_016873584.1:p.Pro604=
|
|
XM_024448629.1:c.2532A>C
|
XP_024304397.1:p.Pro844=
|
|
XM_024448630.1:c.2463A>C
|
XP_024304398.1:p.Pro821=
|
|
XM_024448631.1:c.2400A>C
|
XP_024304399.1:p.Pro800=
|
|
XM_024448633.1:c.2001A>C
|
XP_024304401.1:p.Pro667=
|
|
XR_002957155.1:n.2626A>C
|
|
|
NM_004579.5:c.2412A>C
MANE Select
|
NP_004570.2:p.Pro804=
|
|
NM_001307990.2:c.2388A>C
|
NP_001294919.1:p.Pro796=
|
|