ENST00000358691.10:c.3292T>C
MANE Select
|
ENSP00000351524.5:p.Tyr1098His
|
|
ENST00000358691.9:c.3292T>C
|
ENSP00000351524.5:p.Tyr1098His
|
|
ENST00000579953.5:c.3295T>C
|
ENSP00000463727.1:p.Tyr1099His
|
|
ENST00000580168.5:c.3295T>C
|
ENSP00000464512.1:p.Tyr1099His
|
|
NM_014877.3:c.3292T>C
|
NP_055692.2:p.Tyr1098His
|
|
XM_005257888.3:c.3373T>C
|
XP_005257945.1:p.Tyr1125His
|
|
XM_005257889.3:c.3295T>C
|
XP_005257946.1:p.Tyr1099His
|
|
XM_005257890.3:c.3271T>C
|
XP_005257947.1:p.Tyr1091His
|
|
XM_006722214.2:c.3376T>C
|
XP_006722277.1:p.Tyr1126His
|
|
XM_006722215.2:c.2671T>C
|
XP_006722278.1:p.Tyr891His
|
|
XM_006722216.2:c.2200T>C
|
XP_006722279.1:p.Tyr734His
|
|
XM_011525544.1:c.3376T>C
|
XP_011523846.1:p.Tyr1126His
|
|
XM_011525545.1:c.3376T>C
|
XP_011523847.1:p.Tyr1126His
|
|
XR_934629.1:n.3367T>C
|
|
|
NM_001330447.1:c.3295T>C
|
NP_001317376.1:p.Tyr1099His
|
|
XM_005257888.5:c.3373T>C
|
XP_005257945.1:p.Tyr1125His
|
|
XM_006722214.4:c.3376T>C
|
XP_006722277.1:p.Tyr1126His
|
|
XM_006722215.3:c.2671T>C
|
XP_006722278.1:p.Tyr891His
|
|
XM_006722216.3:c.2200T>C
|
XP_006722279.1:p.Tyr734His
|
|
XM_011525544.2:c.3376T>C
|
XP_011523846.1:p.Tyr1126His
|
|
XM_017025477.2:c.2587T>C
|
XP_016880966.1:p.Tyr863His
|
|
XM_017025478.1:c.2119T>C
|
XP_016880967.1:p.Tyr707His
|
|
XR_001752712.2:n.3467T>C
|
|
|
XR_001752713.2:n.3319T>C
|
|
|
XR_001752714.2:n.3235T>C
|
|
|
NM_014877.4:c.3292T>C
MANE Select
|
NP_055692.3:p.Tyr1098His
|
|
NM_001330447.2:c.3295T>C
|
NP_001317376.2:p.Tyr1099His
|
|