ENST00000559133.6:c.*486C>A
|
ENSP00000453958.2:n.*486C>A
|
|
ENST00000674301.2:c.*1191C>A
|
ENSP00000501333.2:n.*1191C>A
|
|
ENST00000682170.1:n.1859C>A
|
|
|
ENST00000682767.1:n.975C>A
|
|
|
ENST00000316623.10:c.7678C>A
MANE Select
|
ENSP00000325527.5:p.Gln2560Lys
|
|
ENST00000674301.1:c.2844C>A
|
ENSP00000501333.1:n.2844C>A
|
|
ENST00000316623.9:c.7678C>A
|
ENSP00000325527.5:p.Gln2560Lys
|
|
ENST00000559133.5:c.3047C>A
|
|
|
NM_000138.4:c.7678C>A , LRG_778t1:c.7678C>A
|
NP_000129.3:p.Gln2560Lys
|
|
NM_000138.5:c.7678C>A
MANE Select
|
NP_000129.3:p.Gln2560Lys
|
|