|
ENST00000703936.1:c.2740C>G
|
ENSP00000515567.1:p.Pro914Ala
|
|
|
ENST00000703937.1:c.*1801C>G
|
ENSP00000515568.1:n.*1801C>G
|
|
|
ENST00000326739.9:c.700C>G
MANE Select
|
ENSP00000321584.4:p.Pro234Ala
|
|
|
ENST00000429182.6:c.700C>G
|
ENSP00000393525.2:p.Pro234Ala
|
|
|
ENST00000442157.2:c.625C>G
|
ENSP00000403502.2:p.Pro209Ala
|
|
|
ENST00000462980.2:n.1215C>G
|
|
|
|
ENST00000472328.2:n.766C>G
|
|
|
|
ENST00000491610.2:n.660C>G
|
|
|
|
ENST00000676607.1:n.996C>G
|
|
|
|
ENST00000676627.1:n.1430C>G
|
|
|
|
ENST00000676708.1:n.1980C>G
|
|
|
|
ENST00000676864.1:n.1849C>G
|
|
|
|
ENST00000677010.1:c.736C>G
|
ENSP00000503089.1:p.Pro246Ala
|
|
|
ENST00000677108.1:n.2606C>G
|
|
|
|
ENST00000677168.1:n.1172C>G
|
|
|
|
ENST00000677185.1:n.1263C>G
|
|
|
|
ENST00000677205.1:n.1484C>G
|
|
|
|
ENST00000677344.1:n.1974C>G
|
|
|
|
ENST00000677480.1:c.*377C>G
|
ENSP00000504378.1:n.*377C>G
|
|
|
ENST00000677519.1:n.1410C>G
|
|
|
|
ENST00000677593.1:n.1256C>G
|
|
|
|
ENST00000677740.1:n.2205C>G
|
|
|
|
ENST00000677991.1:n.1873C>G
|
|
|
|
ENST00000678001.1:n.1193C>G
|
|
|
|
ENST00000678085.1:n.1256C>G
|
|
|
|
ENST00000678177.1:n.2549C>G
|
|
|
|
ENST00000678603.1:n.1778C>G
|
|
|
|
ENST00000678724.1:c.625C>G
|
ENSP00000503874.1:p.Pro209Ala
|
|
|
ENST00000678920.1:n.858C>G
|
|
|
|
ENST00000679019.1:n.1470C>G
|
|
|
|
ENST00000679117.1:c.*515C>G
|
ENSP00000503240.1:n.*515C>G
|
|
|
ENST00000679339.1:n.1541C>G
|
|
|
|
ENST00000326739.8:c.700C>G
|
ENSP00000321584.4:p.Pro234Ala
|
|
|
ENST00000429182.5:c.494C>G
|
|
|
|
ENST00000442157.1:c.625C>G
|
ENSP00000403502.1:p.Pro209Ala
|
|
|
ENST00000462980.1:n.602C>G
|
|
|
|
ENST00000491610.1:n.660C>G
|
|
|
|
NM_000884.2:c.700C>G
|
NP_000875.2:p.Pro234Ala
|
|
|
XM_006713128.2:c.910C>G
|
XP_006713191.1:p.Pro304Ala
|
|
|
XM_006713128.3:c.910C>G
|
XP_006713191.1:p.Pro304Ala
|
|
|
XM_017006349.1:c.835C>G
|
XP_016861838.1:p.Pro279Ala
|
|
|
XM_017006350.1:c.835C>G
|
XP_016861839.1:p.Pro279Ala
|
|
|
NM_000884.3:c.700C>G
MANE Select
|
NP_000875.2:p.Pro234Ala
|
|
