ENST00000559133.6:c.*507G>C
|
ENSP00000453958.2:n.*507G>C
|
|
ENST00000674301.2:c.*1212G>C
|
ENSP00000501333.2:n.*1212G>C
|
|
ENST00000682170.1:n.1880G>C
|
|
|
ENST00000682767.1:n.996G>C
|
|
|
ENST00000316623.10:c.7699G>C
MANE Select
|
ENSP00000325527.5:p.Asp2567His
|
|
ENST00000674301.1:c.2865G>C
|
ENSP00000501333.1:n.2865G>C
|
|
ENST00000316623.9:c.7699G>C
|
ENSP00000325527.5:p.Asp2567His
|
|
ENST00000559133.5:c.3068G>C
|
|
|
NM_000138.4:c.7699G>C , LRG_778t1:c.7699G>C
|
NP_000129.3:p.Asp2567His
|
|
NM_000138.5:c.7699G>C
MANE Select
|
NP_000129.3:p.Asp2567His
|
|