ENST00000644269.2:c.1454C>G
MANE Select
|
ENSP00000494017.1:p.Thr485Arg
|
|
ENST00000644846.1:c.165C>G
|
|
|
ENST00000265715.7:c.1454C>G
|
ENSP00000265715.3:p.Thr485Arg
|
|
ENST00000460748.1:n.557C>G
|
|
|
ENST00000477350.5:n.301C>G
|
|
|
ENST00000480841.5:n.303C>G
|
|
|
ENST00000497446.5:n.469C>G
|
|
|
NM_000441.1:c.1454C>G
|
NP_000432.1:p.Thr485Arg
|
|
XM_005250425.1:c.1454C>G
|
XP_005250482.1:p.Thr485Arg
|
|
XM_005250425.2:c.1454C>G
|
XP_005250482.1:p.Thr485Arg
|
|
XM_017012318.1:c.1376C>G
|
XP_016867807.1:p.Thr459Arg
|
|
NM_000441.2:c.1454C>G
MANE Select
|
NP_000432.1:p.Thr485Arg
|
|