ENST00000358691.10:c.3262C>T
MANE Select
|
ENSP00000351524.5:p.Gln1088Ter
|
|
ENST00000358691.9:c.3262C>T
|
ENSP00000351524.5:p.Gln1088Ter
|
|
ENST00000579953.5:c.3265C>T
|
ENSP00000463727.1:p.Gln1089Ter
|
|
ENST00000580168.5:c.3265C>T
|
ENSP00000464512.1:p.Gln1089Ter
|
|
NM_014877.3:c.3262C>T
|
NP_055692.2:p.Gln1088Ter
|
|
XM_005257888.3:c.3343C>T
|
XP_005257945.1:p.Gln1115Ter
|
|
XM_005257889.3:c.3265C>T
|
XP_005257946.1:p.Gln1089Ter
|
|
XM_005257890.3:c.3241C>T
|
XP_005257947.1:p.Gln1081Ter
|
|
XM_006722214.2:c.3346C>T
|
XP_006722277.1:p.Gln1116Ter
|
|
XM_006722215.2:c.2641C>T
|
XP_006722278.1:p.Gln881Ter
|
|
XM_006722216.2:c.2170C>T
|
XP_006722279.1:p.Gln724Ter
|
|
XM_011525544.1:c.3346C>T
|
XP_011523846.1:p.Gln1116Ter
|
|
XM_011525545.1:c.3346C>T
|
XP_011523847.1:p.Gln1116Ter
|
|
XR_934629.1:n.3337C>T
|
|
|
NM_001330447.1:c.3265C>T
|
NP_001317376.1:p.Gln1089Ter
|
|
XM_005257888.5:c.3343C>T
|
XP_005257945.1:p.Gln1115Ter
|
|
XM_006722214.4:c.3346C>T
|
XP_006722277.1:p.Gln1116Ter
|
|
XM_006722215.3:c.2641C>T
|
XP_006722278.1:p.Gln881Ter
|
|
XM_006722216.3:c.2170C>T
|
XP_006722279.1:p.Gln724Ter
|
|
XM_011525544.2:c.3346C>T
|
XP_011523846.1:p.Gln1116Ter
|
|
XM_017025477.2:c.2557C>T
|
XP_016880966.1:p.Gln853Ter
|
|
XM_017025478.1:c.2089C>T
|
XP_016880967.1:p.Gln697Ter
|
|
XR_001752712.2:n.3437C>T
|
|
|
XR_001752713.2:n.3289C>T
|
|
|
XR_001752714.2:n.3205C>T
|
|
|
NM_014877.4:c.3262C>T
MANE Select
|
NP_055692.3:p.Gln1088Ter
|
|
NM_001330447.2:c.3265C>T
|
NP_001317376.2:p.Gln1089Ter
|
|