ENST00000264276.11:c.3698G>C
MANE Select
|
ENSP00000264276.6:p.Gly1233Ala
|
|
ENST00000439495.6:c.1376G>C
|
ENSP00000403832.2:p.Gly459Ala
|
|
ENST00000482891.6:n.4466G>C
|
|
|
ENST00000494017.6:n.1430G>C
|
|
|
ENST00000679409.1:c.1376G>C
|
ENSP00000506531.1:p.Gly459Ala
|
|
ENST00000679416.1:n.5202G>C
|
|
|
ENST00000679435.1:c.3698G>C
|
ENSP00000505218.1:p.Gly1233Ala
|
|
ENST00000679516.1:c.3698G>C
|
ENSP00000505187.1:p.Gly1233Ala
|
|
ENST00000679618.1:c.*786G>C
|
ENSP00000506274.1:n.*786G>C
|
|
ENST00000679630.1:n.5547G>C
|
|
|
ENST00000679686.1:n.3812G>C
|
|
|
ENST00000679701.1:n.6690G>C
|
|
|
ENST00000679916.1:c.3698G>C
|
ENSP00000506172.1:p.Gly1233Ala
|
|
ENST00000680000.1:c.3698G>C
|
ENSP00000506173.1:p.Gly1233Ala
|
|
ENST00000680135.1:c.*1662G>C
|
ENSP00000506211.1:n.*1662G>C
|
|
ENST00000680149.1:c.3698G>C
|
ENSP00000506497.1:p.Gly1233Ala
|
|
ENST00000680163.1:c.3698G>C
|
ENSP00000505092.1:p.Gly1233Ala
|
|
ENST00000680174.1:n.4389G>C
|
|
|
ENST00000680236.1:c.*759G>C
|
ENSP00000506212.1:n.*759G>C
|
|
ENST00000680497.1:c.3800G>C
|
ENSP00000505954.1:p.Gly1267Ala
|
|
ENST00000680508.1:c.3698G>C
|
ENSP00000505749.1:p.Gly1233Ala
|
|
ENST00000680569.1:c.*1409G>C
|
ENSP00000505522.1:n.*1409G>C
|
|
ENST00000680630.1:n.4130G>C
|
|
|
ENST00000680634.1:n.21-2558G>C
|
|
|
ENST00000680722.1:n.1498G>C
|
|
|
ENST00000680723.1:n.4481G>C
|
|
|
ENST00000680726.1:c.3698G>C
|
ENSP00000505505.1:p.Gly1233Ala
|
|
ENST00000680737.1:n.3969G>C
|
|
|
ENST00000680759.1:c.3698G>C
|
ENSP00000505848.1:p.Gly1233Ala
|
|
ENST00000680814.1:c.3698G>C
|
ENSP00000505710.1:p.Gly1233Ala
|
|
ENST00000680828.1:c.*1270G>C
|
ENSP00000505249.1:n.*1270G>C
|
|
ENST00000680861.1:c.3698G>C
|
ENSP00000505043.1:p.Gly1233Ala
|
|
ENST00000680927.1:c.3698G>C
|
ENSP00000505473.1:p.Gly1233Ala
|
|
ENST00000680939.1:n.4040G>C
|
|
|
ENST00000681152.1:c.3698G>C
|
ENSP00000505388.1:p.Gly1233Ala
|
|
ENST00000681250.1:c.*415G>C
|
ENSP00000505684.1:n.*415G>C
|
|
ENST00000681256.1:c.*1716G>C
|
ENSP00000505446.1:n.*1716G>C
|
|
ENST00000681279.1:n.4466G>C
|
|
|
ENST00000681303.1:c.3698G>C
|
ENSP00000505576.1:p.Gly1233Ala
|
|
ENST00000681307.1:n.4811G>C
|
|
|
ENST00000681461.1:n.4466G>C
|
|
|
ENST00000681495.1:c.1238G>C
|
ENSP00000506085.1:p.Gly413Ala
|
|
ENST00000681558.1:c.1376G>C
|
ENSP00000505568.1:p.Gly459Ala
|
|
ENST00000681619.1:c.3698G>C
|
ENSP00000505071.1:p.Gly1233Ala
|
|
ENST00000681716.1:c.*1409G>C
|
ENSP00000505078.1:n.*1409G>C
|
|
ENST00000681758.1:n.4040G>C
|
|
|
ENST00000681768.1:c.*1362G>C
|
ENSP00000506311.1:n.*1362G>C
|
|
ENST00000681808.1:c.3698G>C
|
ENSP00000505219.1:p.Gly1233Ala
|
|
ENST00000264276.10:c.3698G>C
|
ENSP00000264276.6:p.Gly1233Ala
|
|
ENST00000439495.5:c.1659G>C
|
|
|
ENST00000482891.5:n.3838G>C
|
|
|
ENST00000489440.5:n.519G>C
|
|
|
NM_020919.3:c.3698G>C
|
NP_065970.2:p.Gly1233Ala
|
|
XM_005246709.2:c.3698G>C
|
XP_005246766.1:p.Gly1233Ala
|
|
XM_006712654.1:c.3698G>C
|
XP_006712717.1:p.Gly1233Ala
|
|
XM_006712655.2:c.1634G>C
|
XP_006712718.1:p.Gly545Ala
|
|
XM_011511530.1:c.3359G>C
|
XP_011509832.1:p.Gly1120Ala
|
|
XM_011511531.1:c.3698G>C
|
XP_011509833.1:p.Gly1233Ala
|
|
XR_922974.1:n.3833G>C
|
|
|
XM_006712654.3:c.3698G>C
|
XP_006712717.1:p.Gly1233Ala
|
|
XM_006712655.3:c.1634G>C
|
XP_006712718.1:p.Gly545Ala
|
|
XM_017004569.2:c.3698G>C
|
XP_016860058.1:p.Gly1233Ala
|
|
XM_017004570.2:c.3698G>C
|
XP_016860059.1:p.Gly1233Ala
|
|
XM_017004572.2:c.1316G>C
|
XP_016860061.1:p.Gly439Ala
|
|
XM_024453024.1:c.3359G>C
|
XP_024308792.1:p.Gly1120Ala
|
|
XM_024453025.1:c.1634G>C
|
XP_024308793.1:p.Gly545Ala
|
|
XR_001738864.2:n.3833G>C
|
|
|
XR_001738865.2:n.3833G>C
|
|
|
XR_001738866.2:n.3833G>C
|
|
|
XR_001738867.2:n.3833G>C
|
|
|
XR_002959320.1:n.2889G>C
|
|
|
NM_020919.4:c.3698G>C
MANE Select
|
NP_065970.2:p.Gly1233Ala
|
|