ENST00000225792.10:c.1373C>A
MANE Select
|
ENSP00000225792.5:p.Ser458Tyr
|
|
ENST00000450599.7:c.1373C>A
|
ENSP00000403085.3:p.Ser458Tyr
|
|
ENST00000577922.6:c.1373C>A
|
ENSP00000464337.2:p.Ser458Tyr
|
|
ENST00000578491.2:n.2893C>A
|
|
|
ENST00000579461.2:n.3448C>A
|
|
|
ENST00000580026.6:n.2770C>A
|
|
|
ENST00000582326.2:n.4359C>A
|
|
|
ENST00000583212.2:c.1058C>A
|
ENSP00000463903.2:p.Ser353Tyr
|
|
ENST00000585111.2:c.1373C>A
|
ENSP00000463168.2:p.Ser458Tyr
|
|
ENST00000585317.2:n.3580C>A
|
|
|
ENST00000676575.1:n.2893C>A
|
|
|
ENST00000676581.1:c.*123C>A
|
ENSP00000504407.1:n.*123C>A
|
|
ENST00000676601.1:c.*388C>A
|
ENSP00000504708.1:n.*388C>A
|
|
ENST00000676785.1:c.1373C>A
|
ENSP00000504794.1:p.Ser458Tyr
|
|
ENST00000676969.1:n.2145C>A
|
|
|
ENST00000677726.1:c.*988C>A
|
ENSP00000504260.1:n.*988C>A
|
|
ENST00000678110.1:n.3070C>A
|
|
|
ENST00000678757.1:c.*123C>A
|
ENSP00000504731.1:n.*123C>A
|
|
ENST00000678810.1:n.3204C>A
|
|
|
ENST00000678814.1:c.*209C>A
|
ENSP00000503045.1:n.*209C>A
|
|
ENST00000678890.1:n.3397C>A
|
|
|
ENST00000225792.9:c.1373C>A
|
ENSP00000225792.5:p.Ser458Tyr
|
|
ENST00000450599.6:c.1136C>A
|
ENSP00000403085.2:p.Ser379Tyr
|
|
ENST00000540698.6:c.*985C>A
|
ENSP00000440276.2:n.*985C>A
|
|
ENST00000578758.5:n.406C>A
|
|
|
ENST00000578804.5:c.1373C>A
|
ENSP00000462885.1:p.Ser458Tyr
|
|
ENST00000580026.5:n.886C>A
|
|
|
ENST00000581230.5:n.2779C>A
|
|
|
ENST00000581237.2:n.382C>A
|
|
|
ENST00000581693.5:c.*1090C>A
|
ENSP00000464566.1:n.*1090C>A
|
|
NM_004396.3:c.1373C>A
|
NP_004387.1:p.Ser458Tyr
|
|
XM_005257111.1:c.1373C>A
|
XP_005257168.1:p.Ser458Tyr
|
|
XM_006721738.1:c.1373C>A
|
XP_006721801.1:p.Ser458Tyr
|
|
XM_011524456.1:c.1373C>A
|
XP_011522758.1:p.Ser458Tyr
|
|
XM_011524457.1:c.1217-291C>A
|
XP_011522759.1:n.1217-291C>A
|
|
NM_001320595.1:c.1373C>A
|
NP_001307524.1:p.Ser458Tyr
|
|
NM_001320596.2:c.1373C>A
|
NP_001307525.1:p.Ser458Tyr
|
|
NM_001320597.1:c.1373C>A
|
NP_001307526.1:p.Ser458Tyr
|
|
NM_004396.4:c.1373C>A
|
NP_004387.1:p.Ser458Tyr
|
|
NM_001320595.2:c.1373C>A
|
NP_001307524.1:p.Ser458Tyr
|
|
NM_001320597.2:c.1373C>A
|
NP_001307526.1:p.Ser458Tyr
|
|
NM_004396.5:c.1373C>A
MANE Select
|
NP_004387.1:p.Ser458Tyr
|
|
NM_001320596.3:c.1373C>A
|
NP_001307525.1:p.Ser458Tyr
|
|