ENST00000286657.10:c.1712T>C
MANE Select
|
ENSP00000286657.4:p.Val571Ala
|
|
ENST00000286657.8:c.1712T>C
|
ENSP00000286657.4:p.Val571Ala
|
|
ENST00000622135.1:c.1712T>C
|
ENSP00000480055.1:p.Val571Ala
|
|
NM_014243.2:c.1712T>C
|
NP_055058.2:p.Val571Ala
|
|
XM_011532421.1:c.1655T>C
|
XP_011530723.1:p.Val552Ala
|
|
XM_011532422.1:c.1628T>C
|
XP_011530724.1:p.Val543Ala
|
|
XM_011532423.1:c.1070T>C
|
XP_011530725.1:p.Val357Ala
|
|
XM_011532424.1:c.980T>C
|
XP_011530726.1:p.Val327Ala
|
|
XM_011532421.2:c.1655T>C
|
XP_011530723.1:p.Val552Ala
|
|
XM_011532422.3:c.1628T>C
|
XP_011530724.1:p.Val543Ala
|
|
NM_014243.3:c.1712T>C
MANE Select
|
NP_055058.2:p.Val571Ala
|
|