|
NM_006267.5:c.9215C>T
MANE Select
|
NP_006258.3:p.Ala3072Val
|
|
ENST00000283195.11:c.9215C>T
MANE Select
|
ENSP00000283195.6:p.Ala3072Val
|
|
NM_006267.4:c.9215C>T
|
NP_006258.3:p.Ala3072Val
|
|
ENST00000283195.10:c.9215C>T
|
ENSP00000283195.6:p.Ala3072Val
|
|
ENST00000697737.1:c.3968C>T
|
ENSP00000513426.1:p.Ala1323Val
|
|
ENST00000697740.1:c.3890C>T
|
ENSP00000513427.1:p.Ala1297Val
|
|
ENST00000697744.1:c.4911C>T
|
|
|
ENST00000697745.1:c.4105C>T
|
|
|
ENST00000697746.1:n.5956C>T
|
|
|
ENST00000697747.1:c.1924C>T
|
|
|
ENST00000697748.1:n.4829C>T
|
|
|
ENST00000697749.1:n.2740C>T
|
|
|
ENST00000697750.1:n.1446C>T
|
|
|
ENST00000697751.1:n.1176C>T
|
|
|
XM_005264002.1:c.9317C>T
|
XP_005264059.1:p.Ala3106Val
|
|
XM_005264002.3:c.9317C>T
|
XP_005264059.1:p.Ala3106Val
|
|
XM_005264003.1:c.9293C>T
|
XP_005264060.1:p.Ala3098Val
|
|
XM_005264003.3:c.9293C>T
|
XP_005264060.1:p.Ala3098Val
|
|
XM_005264004.1:c.9239C>T
|
XP_005264061.1:p.Ala3080Val
|
|
XM_005264004.3:c.9239C>T
|
XP_005264061.1:p.Ala3080Val
|
|
XM_005264005.3:c.9239C>T
|
XP_005264062.1:p.Ala3080Val
|
|
XM_005264005.4:c.9239C>T
|
XP_005264062.1:p.Ala3080Val
|
|
XM_005264007.1:c.6389C>T
|
XP_005264064.1:p.Ala2130Val
|
|
XM_005264007.3:c.6389C>T
|
XP_005264064.1:p.Ala2130Val
|
|
XM_011511575.1:c.9314C>T
|
XP_011509877.1:p.Ala3105Val
|
|
XM_011511575.2:c.9314C>T
|
XP_011509877.1:p.Ala3105Val
|
|
XM_011511576.1:c.9140C>T
|
XP_011509878.1:p.Ala3047Val
|
|
XM_011511576.3:c.9140C>T
|
XP_011509878.1:p.Ala3047Val
|
|
XM_011511577.1:c.6605C>T
|
XP_011509879.1:p.Ala2202Val
|
|
XM_011511578.1:c.6386C>T
|
XP_011509880.1:p.Ala2129Val
|
|
XM_011511578.2:c.6386C>T
|
XP_011509880.1:p.Ala2129Val
|
|
XM_017004623.2:c.8370+9662C>T
|
XP_016860112.1:n.8370+9662C>T
|
