ENST00000684976.1:c.687G>C
MANE Select
|
ENSP00000510011.1:p.Gly229=
|
|
ENST00000643089.1:c.687G>C
|
ENSP00000496594.1:p.Gly229=
|
|
ENST00000339174.9:c.627G>C
|
ENSP00000342535.5:p.Gly209=
|
|
ENST00000355905.6:c.627G>C
|
ENSP00000348169.2:p.Gly209=
|
|
ENST00000382868.5:c.798G>C
|
ENSP00000372320.1:p.Gly266=
|
|
ENST00000382872.5:c.123G>C
|
ENSP00000372325.1:p.Gly41=
|
|
ENST00000476359.1:n.1172G>C
|
|
|
NM_001206850.1:c.123G>C
|
NP_001193779.1:p.Gly41=
|
|
NM_014893.4:c.627G>C
|
NP_055708.3:p.Gly209=
|
|
NR_028319.1:n.1101G>C
|
|
|
NR_046355.1:n.866G>C
|
|
|
XM_006724874.1:c.687G>C
|
XP_006724937.1:p.Gly229=
|
|
XM_011531424.1:c.687G>C
|
XP_011529726.1:p.Gly229=
|
|
XM_011531425.1:c.687G>C
|
XP_011529727.1:p.Gly229=
|
|
XM_011531426.1:c.687G>C
|
XP_011529728.1:p.Gly229=
|
|
XM_011531427.1:c.687G>C
|
XP_011529729.1:p.Gly229=
|
|
XM_011531428.1:c.687G>C
|
XP_011529730.1:p.Gly229=
|
|
XM_011531429.1:c.687G>C
|
XP_011529731.1:p.Gly229=
|
|
XM_011531430.1:c.687G>C
|
XP_011529732.1:p.Gly229=
|
|
NM_001365584.1:c.687G>C
|
NP_001352513.1:p.Gly229=
|
|
NM_001365586.1:c.687G>C
|
NP_001352515.1:p.Gly229=
|
|
NM_001365588.1:c.687G>C
MANE Select
|
NP_001352517.1:p.Gly229=
|
|
NM_001365590.1:c.627G>C
|
NP_001352519.1:p.Gly209=
|
|
NM_001365591.1:c.627G>C
|
NP_001352520.1:p.Gly209=
|
|
NM_001365592.1:c.627G>C
|
NP_001352521.1:p.Gly209=
|
|
NM_001365593.1:c.627G>C
|
NP_001352522.1:p.Gly209=
|
|
XM_006724874.2:c.687G>C
|
XP_006724937.1:p.Gly229=
|
|
XM_011531427.2:c.687G>C
|
XP_011529729.1:p.Gly229=
|
|
XM_011531429.2:c.687G>C
|
XP_011529731.1:p.Gly229=
|
|
XM_011531430.2:c.687G>C
|
XP_011529732.1:p.Gly229=
|
|
XM_017030036.1:c.627G>C
|
XP_016885525.1:p.Gly209=
|
|
XM_017030039.1:c.252G>C
|
XP_016885528.1:p.Gly84=
|
|
XM_017030040.1:c.123G>C
|
XP_016885529.1:p.Gly41=
|
|
XM_024452490.1:c.687G>C
|
XP_024308258.1:p.Gly229=
|
|
NM_001206850.2:c.123G>C
|
NP_001193779.1:p.Gly41=
|
|
NM_014893.5:c.627G>C
|
NP_055708.3:p.Gly209=
|
|
NR_046355.2:n.866G>C
|
|
|
NM_001394830.1:c.687G>C
|
NP_001381759.1:p.Gly229=
|
|
NM_001394831.1:c.627G>C
|
NP_001381760.1:p.Gly209=
|
|