ENST00000559133.6:c.*234C>G
|
ENSP00000453958.2:n.*234C>G
|
|
ENST00000674301.2:c.*939C>G
|
ENSP00000501333.2:n.*939C>G
|
|
ENST00000682170.1:n.1607C>G
|
|
|
ENST00000682767.1:n.723C>G
|
|
|
ENST00000316623.10:c.7426C>G
MANE Select
|
ENSP00000325527.5:p.Leu2476Val
|
|
ENST00000674301.1:c.2592C>G
|
ENSP00000501333.1:n.2592C>G
|
|
ENST00000316623.9:c.7426C>G
|
ENSP00000325527.5:p.Leu2476Val
|
|
ENST00000559133.5:c.2795C>G
|
|
|
NM_000138.4:c.7426C>G , LRG_778t1:c.7426C>G
|
NP_000129.3:p.Leu2476Val
|
|
NM_000138.5:c.7426C>G
MANE Select
|
NP_000129.3:p.Leu2476Val
|
|