ENST00000530449.2:n.195G>T
|
|
|
ENST00000698254.1:c.1099G>T
|
ENSP00000513629.1:p.Ala367Ser
|
|
ENST00000698255.1:c.1519G>T
|
ENSP00000513630.1:p.Ala507Ser
|
|
ENST00000698256.1:c.1036G>T
|
|
|
ENST00000698257.1:n.988G>T
|
|
|
ENST00000698258.1:n.705G>T
|
|
|
ENST00000698259.1:n.471G>T
|
|
|
ENST00000265686.8:c.1570G>T
MANE Select
|
ENSP00000265686.3:p.Ala524Ser
|
|
ENST00000265686.7:c.1570G>T
|
ENSP00000265686.3:p.Ala524Ser
|
|
ENST00000525724.5:n.882G>T
|
|
|
ENST00000528981.5:c.722G>T
|
|
|
ENST00000532635.5:c.922G>T
|
ENSP00000434407.1:p.Ala308Ser
|
|
ENST00000533005.5:n.683G>T
|
|
|
NM_006019.3:c.1570G>T
|
NP_006010.2:p.Ala524Ser
|
|
NM_006053.3:c.922G>T
|
NP_006044.1:p.Ala308Ser
|
|
XM_005273709.2:c.1570G>T
|
XP_005273766.1:p.Ala524Ser
|
|
XM_011544726.1:c.1570G>T
|
XP_011543028.1:p.Ala524Ser
|
|
XM_011544727.1:c.1570G>T
|
XP_011543029.1:p.Ala524Ser
|
|
XM_011544728.1:c.1570G>T
|
XP_011543030.1:p.Ala524Ser
|
|
XR_949754.1:n.1574G>T
|
|
|
NM_001351059.1:c.676G>T
|
NP_001337988.1:p.Ala226Ser
|
|
XM_024448320.1:c.1663G>T
|
XP_024304088.1:p.Ala555Ser
|
|
XM_024448321.1:c.1663G>T
|
XP_024304089.1:p.Ala555Ser
|
|
XM_024448322.1:c.1663G>T
|
XP_024304090.1:p.Ala555Ser
|
|
XM_024448323.1:c.1663G>T
|
XP_024304091.1:p.Ala555Ser
|
|
XM_024448324.1:c.1663G>T
|
XP_024304092.1:p.Ala555Ser
|
|
XR_001747721.2:n.1694G>T
|
|
|
XR_001747722.1:n.1707G>T
|
|
|
XR_001747723.2:n.1707G>T
|
|
|
XR_002957115.1:n.1785G>T
|
|
|
NM_006019.4:c.1570G>T
MANE Select
|
NP_006010.2:p.Ala524Ser
|
|
NM_001351059.2:c.676G>T
|
NP_001337988.1:p.Ala226Ser
|
|
NM_006053.4:c.922G>T
|
NP_006044.1:p.Ala308Ser
|
|