ENST00000690565.1:c.1454G>C
|
ENSP00000510501.1:p.Gly485Ala
|
|
ENST00000691308.1:c.829-155G>C
|
ENSP00000509583.1:n.829-155G>C
|
|
ENST00000448666.7:c.1454G>C
MANE Select
|
ENSP00000410992.3:p.Gly485Ala
|
|
ENST00000452063.7:c.1136G>C
|
ENSP00000388201.2:p.Gly379Ala
|
|
ENST00000462443.2:c.629G>C
|
ENSP00000497265.1:p.Gly210Ala
|
|
ENST00000647723.1:c.1397G>C
|
|
|
ENST00000647753.1:c.*747G>C
|
ENSP00000497318.1:n.*747G>C
|
|
ENST00000647771.1:c.*942G>C
|
ENSP00000496788.1:n.*942G>C
|
|
ENST00000647915.1:c.*747G>C
|
ENSP00000498123.1:n.*747G>C
|
|
ENST00000648768.1:n.1711G>C
|
|
|
ENST00000648810.1:c.629G>C
|
ENSP00000496949.1:p.Gly210Ala
|
|
ENST00000649075.1:c.*382G>C
|
ENSP00000497836.1:n.*382G>C
|
|
ENST00000649601.1:c.*634G>C
|
ENSP00000496796.1:n.*634G>C
|
|
ENST00000649777.1:n.1663G>C
|
|
|
ENST00000649854.1:c.1087G>C
|
|
|
ENST00000650523.1:c.1229G>C
|
ENSP00000497143.1:p.Gly410Ala
|
|
ENST00000233616.8:c.1454G>C
|
ENSP00000233616.4:p.Gly485Ala
|
|
ENST00000409065.5:c.*634G>C
|
ENSP00000386493.1:n.*634G>C
|
|
ENST00000448666.5:c.1136G>C
|
ENSP00000410992.1:p.Gly379Ala
|
|
ENST00000452063.6:c.1136G>C
|
ENSP00000388201.2:p.Gly379Ala
|
|
ENST00000462189.1:n.1135G>C
|
|
|
NM_001146158.1:c.1136G>C
|
NP_001139630.1:p.Gly379Ala
|
|
NM_006302.2:c.1454G>C
|
NP_006293.2:p.Gly485Ala
|
|
NM_006302.3:c.1454G>C
MANE Select
|
NP_006293.2:p.Gly485Ala
|
|
NM_001146158.2:c.1136G>C
|
NP_001139630.1:p.Gly379Ala
|
|