|
NM_001002294.3:c.1499G>A
MANE Select
|
NP_001002294.1:p.Arg500Gln
|
|
ENST00000367755.9:c.1499G>A
MANE Select
|
ENSP00000356729.4:p.Arg500Gln
|
|
NM_001002294.2:c.1499G>A
|
NP_001002294.1:p.Arg500Gln
|
|
NM_001319173.1:c.1439G>A
|
NP_001306102.1:p.Arg480Gln
|
|
NM_001319173.2:c.1439G>A
|
NP_001306102.1:p.Arg480Gln
|
|
NM_001319174.1:c.1310G>A
|
NP_001306103.1:p.Arg437Gln
|
|
NM_001319174.2:c.1310G>A
|
NP_001306103.1:p.Arg437Gln
|
|
NM_006894.5:c.1499G>A
|
NP_008825.4:p.Arg500Gln
|
|
NM_006894.6:c.1499G>A
|
NP_008825.4:p.Arg500Gln
|
|
ENST00000367755.8:c.1499G>A
|
ENSP00000356729.4:p.Arg500Gln
|
|
XM_005245044.1:c.1310G>A
|
XP_005245101.1:p.Arg437Gln
|
|
XM_011509345.1:c.1439G>A
|
XP_011507647.1:p.Arg480Gln
|
|
XM_011509345.3:c.1439G>A
|
XP_011507647.1:p.Arg480Gln
|
|
XM_011509346.1:c.1439G>A
|
XP_011507648.1:p.Arg480Gln
|
|
XM_024454365.1:c.752G>A
|
XP_024310133.1:p.Arg251Gln
|