ENST00000559133.6:c.*878G>T
|
ENSP00000453958.2:n.*878G>T
|
|
ENST00000674301.2:c.*1583G>T
|
ENSP00000501333.2:n.*1583G>T
|
|
ENST00000682158.1:n.1451G>T
|
|
|
ENST00000682170.1:n.2251G>T
|
|
|
ENST00000682767.1:n.1367G>T
|
|
|
ENST00000316623.10:c.8070G>T
MANE Select
|
ENSP00000325527.5:p.Met2690Ile
|
|
ENST00000674301.1:c.3236G>T
|
ENSP00000501333.1:n.3236G>T
|
|
ENST00000316623.9:c.8070G>T
|
ENSP00000325527.5:p.Met2690Ile
|
|
ENST00000559133.5:c.3439G>T
|
|
|
ENST00000561429.1:n.325G>T
|
|
|
NM_000138.4:c.8070G>T , LRG_778t1:c.8070G>T
|
NP_000129.3:p.Met2690Ile
|
|
NM_000138.5:c.8070G>T
MANE Select
|
NP_000129.3:p.Met2690Ile
|
|