ENST00000378156.9:c.4107G>C
MANE Select
|
ENSP00000367398.4:p.Pro1369=
|
|
ENST00000378156.8:c.4107G>C
|
ENSP00000367398.4:p.Pro1369=
|
|
ENST00000378161.5:n.3258G>C
|
|
|
ENST00000378169.7:c.*3008G>C
|
ENSP00000367411.3:n.*3008G>C
|
|
ENST00000460696.1:n.2855G>C
|
|
|
ENST00000478423.6:n.3839G>C
|
|
|
ENST00000489180.6:c.*1918G>C
|
ENSP00000423747.1:n.*1918G>C
|
|
NM_001291593.1:c.2568G>C
|
NP_001278522.1:p.Pro856=
|
|
NM_001291594.1:c.2571G>C
|
NP_001278523.1:p.Pro857=
|
|
NM_015102.4:c.4107G>C
|
NP_055917.1:p.Pro1369=
|
|
NR_111987.1:n.4922G>C
|
|
|
XM_006710563.2:c.4107G>C
|
XP_006710626.1:p.Pro1369=
|
|
XM_006710565.2:c.4107G>C
|
XP_006710628.1:p.Pro1369=
|
|
XM_011541213.1:c.4104G>C
|
XP_011539515.1:p.Pro1368=
|
|
XM_011541214.1:c.4065G>C
|
XP_011539516.1:p.Pro1355=
|
|
XM_011541215.1:c.3996G>C
|
XP_011539517.1:p.Pro1332=
|
|
XM_011541216.1:c.4107G>C
|
XP_011539518.1:p.Pro1369=
|
|
XM_011541217.1:c.4107G>C
|
XP_011539519.1:p.Pro1369=
|
|
XM_011541218.1:c.4107G>C
|
XP_011539520.1:p.Pro1369=
|
|
XM_011541219.1:c.4053G>C
|
XP_011539521.1:p.Pro1351=
|
|
XM_006710563.3:c.4107G>C
|
XP_006710626.1:p.Pro1369=
|
|
XM_011541216.2:c.4107G>C
|
XP_011539518.1:p.Pro1369=
|
|
XM_011541217.2:c.4107G>C
|
XP_011539519.1:p.Pro1369=
|
|
XM_011541218.2:c.4107G>C
|
XP_011539520.1:p.Pro1369=
|
|
XM_017000996.1:c.4062G>C
|
XP_016856485.1:p.Pro1354=
|
|
XM_017000997.1:c.4107G>C
|
XP_016856486.1:p.Pro1369=
|
|
XM_017000999.1:c.3579G>C
|
XP_016856488.1:p.Pro1193=
|
|
XM_017001000.2:c.3579G>C
|
XP_016856489.1:p.Pro1193=
|
|
XM_017001001.1:c.3309G>C
|
XP_016856490.1:p.Pro1103=
|
|
XM_017001003.1:c.2568G>C
|
XP_016856492.1:p.Pro856=
|
|
XR_001737114.1:n.3973G>C
|
|
|
XR_001737115.1:n.3958G>C
|
|
|
NM_015102.5:c.4107G>C
MANE Select
|
NP_055917.1:p.Pro1369=
|
|
NM_001291593.2:c.2568G>C
|
NP_001278522.1:p.Pro856=
|
|
NM_001291594.2:c.2571G>C
|
NP_001278523.1:p.Pro857=
|
|
NR_111987.2:n.4874G>C
|
|
|