ENST00000642192.1:c.-270G>T
|
ENSP00000494225.1:n.-270G>T
|
|
ENST00000642492.1:c.-371G>T
|
ENSP00000496267.1:n.-371G>T
|
|
ENST00000643738.1:c.-270G>T
|
ENSP00000493684.1:n.-270G>T
|
|
ENST00000644554.1:c.-270G>T
|
ENSP00000495037.1:n.-270G>T
|
|
ENST00000644580.2:c.208G>T
MANE Select
|
ENSP00000495855.2:p.Ala70Ser
|
|
ENST00000645572.1:c.208G>T
|
ENSP00000494301.1:p.Ala70Ser
|
|
ENST00000645762.1:n.322G>T
|
|
|
ENST00000645817.1:c.-270G>T
|
ENSP00000495731.1:n.-270G>T
|
|
ENST00000647226.1:c.-270G>T
|
ENSP00000496024.1:n.-270G>T
|
|
ENST00000375129.8:c.208G>T
|
ENSP00000364271.4:p.Ala70Ser
|
|
ENST00000409117.7:c.208G>T
|
ENSP00000386647.3:p.Ala70Ser
|
|
ENST00000437056.5:n.367G>T
|
|
|
ENST00000442710.5:c.50G>T
|
|
|
NM_001042702.3:c.208G>T
|
NP_001036167.1:p.Ala70Ser
|
|
XM_005246627.1:c.217G>T
|
XP_005246684.1:p.Ala73Ser
|
|
XM_005246628.2:c.313G>T
|
XP_005246685.1:p.Ala105Ser
|
|
XM_005246629.2:c.199G>T
|
XP_005246686.1:p.Ala67Ser
|
|
XM_011511247.1:c.313G>T
|
XP_011509549.1:p.Ala105Ser
|
|
XM_011511248.1:c.277G>T
|
XP_011509550.1:p.Ala93Ser
|
|
XM_011511249.1:c.-266-715G>T
|
XP_011509551.1:n.-266-715G>T
|
|
XM_011511250.1:c.-270G>T
|
XP_011509552.1:n.-270G>T
|
|
XM_011511251.1:c.-266-715G>T
|
XP_011509553.1:n.-266-715G>T
|
|
XR_922929.1:n.980G>T
|
|
|
NM_001042702.4:c.208G>T
|
NP_001036167.1:p.Ala70Ser
|
|
NM_001353775.1:c.217G>T
|
NP_001340704.1:p.Ala73Ser
|
|
NM_001353776.1:c.313G>T
|
NP_001340705.1:p.Ala105Ser
|
|
NM_001353777.1:c.-270G>T
|
NP_001340706.1:n.-270G>T
|
|
NM_001353778.1:c.-270G>T
|
NP_001340707.1:n.-270G>T
|
|
XM_005246629.4:c.199G>T
|
XP_005246686.1:p.Ala67Ser
|
|
XM_011511247.3:c.313G>T
|
XP_011509549.1:p.Ala105Ser
|
|
XM_011511249.3:c.-266-715G>T
|
XP_011509551.1:n.-266-715G>T
|
|
XM_017004221.2:c.313G>T
|
XP_016859710.1:p.Ala105Ser
|
|
XM_017004224.2:c.-981G>T
|
XP_016859713.1:n.-981G>T
|
|
XM_024452927.1:c.-371G>T
|
XP_024308695.1:n.-371G>T
|
|
XM_024452928.1:c.-270G>T
|
XP_024308696.1:n.-270G>T
|
|
XR_001738753.2:n.2020G>T
|
|
|
XR_002959300.1:n.2020G>T
|
|
|
XR_922929.3:n.503G>T
|
|
|
NM_001042702.5:c.208G>T
MANE Select
|
NP_001036167.1:p.Ala70Ser
|
|
NM_001369912.1:c.208G>T
|
NP_001356841.1:p.Ala70Ser
|
|
NM_001353775.2:c.217G>T
|
NP_001340704.1:p.Ala73Ser
|
|
NM_001353776.2:c.313G>T
|
NP_001340705.1:p.Ala105Ser
|
|
NM_001353778.2:c.-270G>T
|
NP_001340707.1:n.-270G>T
|
|