ENST00000299084.9:c.817A>G
MANE Select
|
ENSP00000299084.4:p.Arg273Gly
|
|
ENST00000299084.8:c.817A>G
|
ENSP00000299084.4:p.Arg273Gly
|
|
NM_152594.2:c.817A>G
|
NP_689807.1:p.Arg273Gly
|
|
XM_005254202.2:c.853A>G
|
XP_005254259.1:p.Arg285Gly
|
|
XM_005254203.3:c.595A>G
|
XP_005254260.1:p.Arg199Gly
|
|
XM_011521288.1:c.754A>G
|
XP_011519590.1:p.Arg252Gly
|
|
XM_011521289.1:c.754A>G
|
XP_011519591.1:p.Arg252Gly
|
|
XM_011521290.1:c.754A>G
|
XP_011519592.1:p.Arg252Gly
|
|
XM_005254202.3:c.853A>G
|
XP_005254259.1:p.Arg285Gly
|
|
XM_011521289.3:c.754A>G
|
XP_011519591.1:p.Arg252Gly
|
|
NM_152594.3:c.817A>G
MANE Select
|
NP_689807.1:p.Arg273Gly
|
|