|
ENST00000369975.6:c.2111G>A
|
ENSP00000358992.1:p.Gly704Asp
|
|
|
ENST00000369977.8:c.2111G>A
MANE Select
|
ENSP00000358994.3:p.Gly704Asp
|
|
|
ENST00000369985.9:c.2111G>A
|
ENSP00000359002.3:p.Gly704Asp
|
|
|
ENST00000462633.3:c.*1667G>A
|
ENSP00000499616.2:n.*1667G>A
|
|
|
ENST00000627432.3:c.2120G>A
|
ENSP00000487348.2:p.Gly707Asp
|
|
|
ENST00000653423.1:c.2111G>A
|
ENSP00000499696.1:p.Gly704Asp
|
|
|
ENST00000653917.1:c.*218G>A
|
ENSP00000499623.1:n.*218G>A
|
|
|
ENST00000660420.1:c.*2067G>A
|
ENSP00000499263.1:n.*2067G>A
|
|
|
ENST00000662184.1:c.*218G>A
|
ENSP00000499732.1:n.*218G>A
|
|
|
ENST00000662603.1:c.2111G>A
|
ENSP00000499324.1:p.Gly704Asp
|
|
|
ENST00000663400.1:c.*136G>A
|
ENSP00000499736.1:n.*136G>A
|
|
|
ENST00000664209.1:c.2111G>A
|
ENSP00000499768.1:p.Gly704Asp
|
|
|
ENST00000664640.1:c.2111G>A
|
ENSP00000499278.1:p.Gly704Asp
|
|
|
ENST00000671923.1:c.*218G>A
|
ENSP00000500835.1:n.*218G>A
|
|
|
ENST00000672093.1:c.2111G>A
|
ENSP00000500710.1:p.Gly704Asp
|
|
|
ENST00000369975.5:c.2111G>A
|
ENSP00000358992.1:p.Gly704Asp
|
|
|
ENST00000369977.7:c.2111G>A
|
ENSP00000358994.3:p.Gly704Asp
|
|
|
ENST00000369981.7:c.2111G>A
|
ENSP00000358998.4:p.Gly704Asp
|
|
|
ENST00000369985.8:c.2111G>A
|
ENSP00000359002.3:p.Gly704Asp
|
|
|
ENST00000462633.1:n.306G>A
|
|
|
|
ENST00000615563.4:c.2111G>A
|
ENSP00000478013.1:p.Gly704Asp
|
|
|
ENST00000627432.2:c.2111G>A
|
ENSP00000487348.1:p.Gly704Asp
|
|
|
NM_001300899.1:c.2111G>A
|
NP_001287828.1:p.Gly704Asp
|
|
|
NM_004999.3:c.2111G>A
|
NP_004990.3:p.Gly704Asp
|
|
|
XM_005248719.2:c.2111G>A
|
XP_005248776.1:p.Gly704Asp
|
|
|
XM_005248720.2:c.2111G>A
|
XP_005248777.1:p.Gly704Asp
|
|
|
XM_005248721.2:c.2111G>A
|
XP_005248778.1:p.Gly704Asp
|
|
|
XM_005248722.2:c.2111G>A
|
XP_005248779.1:p.Gly704Asp
|
|
|
XM_005248724.2:c.2111G>A
|
XP_005248781.1:p.Gly704Asp
|
|
|
XM_005248726.2:c.2111G>A
|
XP_005248783.1:p.Gly704Asp
|
|
|
XM_005248719.4:c.2111G>A
|
XP_005248776.1:p.Gly704Asp
|
|
|
XM_005248720.4:c.2111G>A
|
XP_005248777.1:p.Gly704Asp
|
|
|
XM_005248721.4:c.2111G>A
|
XP_005248778.1:p.Gly704Asp
|
|
|
XM_005248722.4:c.2111G>A
|
XP_005248779.1:p.Gly704Asp
|
|
|
XM_005248724.4:c.2111G>A
|
XP_005248781.1:p.Gly704Asp
|
|
|
XM_005248726.4:c.2111G>A
|
XP_005248783.1:p.Gly704Asp
|
|
|
XM_017010899.2:c.2111G>A
|
XP_016866388.1:p.Gly704Asp
|
|
|
XM_024446447.1:c.2111G>A
|
XP_024302215.1:p.Gly704Asp
|
|
|
XM_024446448.1:c.2111G>A
|
XP_024302216.1:p.Gly704Asp
|
|
|
NM_004999.4:c.2111G>A
MANE Select
|
NP_004990.3:p.Gly704Asp
|
|
|
NM_001300899.2:c.2111G>A
|
NP_001287828.1:p.Gly704Asp
|
|
|
NM_001368136.1:c.2111G>A
|
NP_001355065.1:p.Gly704Asp
|
|
|
NM_001368137.1:c.2111G>A
|
NP_001355066.1:p.Gly704Asp
|
|
|
NM_001368138.1:c.2096G>A
|
NP_001355067.1:p.Gly699Asp
|
|
|
NM_001368865.1:c.2111G>A
|
NP_001355794.1:p.Gly704Asp
|
|
|
NM_001368866.1:c.2111G>A
|
NP_001355795.1:p.Gly704Asp
|
|
|
NR_160538.1:n.2436G>A
|
|
|
