ENST00000449082.3:c.3119_3120insCACT
MANE Select
|
ENSP00000390600.2:p.Asp1041ThrfsTer16
|
|
ENST00000643924.1:c.3116_3117insCACT
|
ENSP00000495595.1:p.Asp1040ThrfsTer16
|
|
ENST00000655275.1:c.3143_3144insCACT
|
ENSP00000499510.1:p.Asp1049ThrfsTer16
|
|
ENST00000449082.2:c.3119_3120insCACT
|
ENSP00000390600.2:p.Asp1041ThrfsTer16
|
|
NM_001293306.2:c.3116_3117insCACT
|
NP_001280235.2:p.Asp1040ThrfsTer16
|
|
NM_001293307.2:c.2825_2826insCACT
|
NP_001280236.2:p.Asp943ThrfsTer16
|
|
NM_006514.3:c.3119_3120insCACT
|
NP_006505.3:p.Asp1041ThrfsTer16
|
|
XM_005265371.2:c.3128_3129insCACT
|
XP_005265428.1:p.Asp1044ThrfsTer16
|
|
XM_011533993.1:c.3125_3126insCACT
|
XP_011532295.1:p.Asp1043ThrfsTer16
|
|
XM_011533994.1:c.2834_2835insCACT
|
XP_011532296.1:p.Asp946ThrfsTer16
|
|
XM_005265371.3:c.3128_3129insCACT
|
XP_005265428.1:p.Asp1044ThrfsTer16
|
|
XM_011533993.2:c.3125_3126insCACT
|
XP_011532295.1:p.Asp1043ThrfsTer16
|
|
XM_011533994.2:c.2834_2835insCACT
|
XP_011532296.1:p.Asp946ThrfsTer16
|
|
NM_006514.4:c.3119_3120insCACT
MANE Select
|
NP_006505.4:p.Asp1041ThrfsTer16
|
|