|
NM_001163435.3:c.1088G>C
MANE Select
|
NP_001156907.2:p.Gly363Ala
|
|
ENST00000394708.7:c.1088G>C
MANE Select
|
ENSP00000378198.2:p.Gly363Ala
|
|
NM_001163435.2:c.1088G>C
|
NP_001156907.1:p.Gly363Ala
|
|
NM_001163436.2:c.1088G>C
|
NP_001156908.1:p.Gly363Ala
|
|
NM_001163436.4:c.1088G>C
|
NP_001156908.2:p.Gly363Ala
|
|
NM_001163437.2:c.971G>C
|
NP_001156909.1:p.Gly324Ala
|
|
NM_001163437.3:c.971G>C
|
NP_001156909.2:p.Gly324Ala
|
|
NM_001290768.1:c.572G>C
|
NP_001277697.1:p.Gly191Ala
|
|
NM_001290768.2:c.572G>C
|
NP_001277697.2:p.Gly191Ala
|
|
NM_033115.4:c.899G>C
|
NP_149106.2:p.Gly300Ala
|
|
NM_033115.5:c.899G>C
|
NP_149106.3:p.Gly300Ala
|
|
ENST00000273980.10:c.1088G>C
|
ENSP00000273980.4:p.Gly363Ala
|
|
ENST00000273980.9:c.1088G>C
|
ENSP00000273980.4:p.Gly363Ala
|
|
ENST00000361687.8:c.899G>C
|
ENSP00000355338.4:p.Gly300Ala
|
|
ENST00000394706.7:c.971G>C
|
ENSP00000378196.3:p.Gly324Ala
|
|
ENST00000394708.6:c.1088G>C
|
ENSP00000378198.2:p.Gly363Ala
|
|
ENST00000432496.6:c.1088G>C
|
ENSP00000405847.2:p.Gly363Ala
|
|
ENST00000467183.6:c.*727G>C
|
ENSP00000421182.1:n.*727G>C
|
|
ENST00000508666.5:c.304G>C
|
|
|
ENST00000510927.5:n.741G>C
|
|
|
XM_006714419.2:c.1088G>C
|
XP_006714482.1:p.Gly363Ala
|
|
XM_011532417.1:c.1088G>C
|
XP_011530719.1:p.Gly363Ala
|
|
XM_011532417.2:c.1088G>C
|
XP_011530719.1:p.Gly363Ala
|
|
XM_011532418.1:c.770G>C
|
XP_011530720.1:p.Gly257Ala
|
|
XM_011532419.1:c.572G>C
|
XP_011530721.1:p.Gly191Ala
|
|
XM_017008846.1:c.1088G>C
|
XP_016864335.1:p.Gly363Ala
|
|
XM_017008847.2:c.1088G>C
|
XP_016864336.1:p.Gly363Ala
|
|
XM_017008848.1:c.770G>C
|
XP_016864337.1:p.Gly257Ala
|
|
XM_017008849.1:c.572G>C
|
XP_016864338.1:p.Gly191Ala
|
|
XM_024454281.1:c.1088G>C
|
XP_024310049.1:p.Gly363Ala
|
|
XM_024454282.1:c.1088G>C
|
XP_024310050.1:p.Gly363Ala
|
|
XR_001741353.2:n.1428G>C
|
|
|
XR_001741354.2:n.1025G>C
|
|
|
XR_002959772.1:n.1212G>C
|
|
|
XR_938800.1:n.1117G>C
|
|
|
XR_938800.3:n.1428G>C
|
|
