ENST00000378823.8:c.3171T>A
MANE Select
|
ENSP00000368100.4:p.His1057Gln
|
|
ENST00000638452.2:c.2874T>A
|
ENSP00000492349.2:p.His958Gln
|
|
ENST00000638504.1:n.2779T>A
|
|
|
ENST00000638568.2:c.2874T>A
|
ENSP00000491158.2:p.His958Gln
|
|
ENST00000639899.1:n.3690T>A
|
|
|
ENST00000640655.2:c.2874T>A
|
ENSP00000491596.2:p.His958Gln
|
|
ENST00000651249.1:c.7T>A
|
|
|
ENST00000378823.7:c.3171T>A
|
ENSP00000368100.4:p.His1057Gln
|
|
ENST00000533482.5:c.*2797T>A
|
ENSP00000431225.1:n.*2797T>A
|
|
NM_005732.3:c.3171T>A
|
NP_005723.2:p.His1057Gln
|
|
NM_005732.4:c.3171T>A
MANE Select
|
NP_005723.2:p.His1057Gln
|
|