ENST00000559133.6:c.6967A>T
|
ENSP00000453958.2:p.Thr2323Ser
|
|
ENST00000674301.2:c.*418A>T
|
ENSP00000501333.2:n.*418A>T
|
|
ENST00000682170.1:n.576A>T
|
|
|
ENST00000682767.1:n.202A>T
|
|
|
ENST00000316623.10:c.6967A>T
MANE Select
|
ENSP00000325527.5:p.Thr2323Ser
|
|
ENST00000674301.1:c.2071A>T
|
ENSP00000501333.1:n.2071A>T
|
|
ENST00000316623.9:c.6967A>T
|
ENSP00000325527.5:p.Thr2323Ser
|
|
ENST00000559133.5:c.2274A>T
|
|
|
ENST00000560720.1:n.254A>T
|
|
|
NM_000138.4:c.6967A>T , LRG_778t1:c.6967A>T
|
NP_000129.3:p.Thr2323Ser
|
|
NM_000138.5:c.6967A>T
MANE Select
|
NP_000129.3:p.Thr2323Ser
|
|