ENST00000559133.6:c.6153A>C
|
ENSP00000453958.2:p.Arg2051Ser
|
|
ENST00000674301.2:c.6153A>C
|
ENSP00000501333.2:p.Arg2051Ser
|
|
ENST00000316623.10:c.6153A>C
MANE Select
|
ENSP00000325527.5:p.Arg2051Ser
|
|
ENST00000674301.1:c.1152A>C
|
ENSP00000501333.1:p.Arg384Ser
|
|
ENST00000316623.9:c.6153A>C
|
ENSP00000325527.5:p.Arg2051Ser
|
|
ENST00000537463.6:c.*1916A>C
|
ENSP00000440294.2:n.*1916A>C
|
|
ENST00000559133.5:c.1460A>C
|
|
|
ENST00000560820.1:n.273A>C
|
|
|
NM_000138.4:c.6153A>C , LRG_778t1:c.6153A>C
|
NP_000129.3:p.Arg2051Ser
|
|
NM_000138.5:c.6153A>C
MANE Select
|
NP_000129.3:p.Arg2051Ser
|
|