ENST00000389857.11:c.5116C>G
MANE Select
|
ENSP00000374507.6:p.Pro1706Ala
|
|
ENST00000331194.8:c.688C>G
|
ENSP00000330332.8:p.Pro230Ala
|
|
ENST00000334448.5:n.928C>G
|
|
|
ENST00000389857.10:c.5116C>G
|
ENSP00000374507.6:p.Pro1706Ala
|
|
ENST00000556726.5:c.1344C>G
|
|
|
NM_001080414.3:c.5116C>G
|
NP_001073883.2:p.Pro1706Ala
|
|
XM_011536796.1:c.5008C>G
|
XP_011535098.1:p.Pro1670Ala
|
|
XR_429316.2:n.5391C>G
|
|
|
XM_011536796.2:c.5008C>G
|
XP_011535098.1:p.Pro1670Ala
|
|
XM_017021336.1:c.2197C>G
|
XP_016876825.1:p.Pro733Ala
|
|
XR_429316.4:n.5389C>G
|
|
|
NM_001080414.4:c.5116C>G
MANE Select
|
NP_001073883.2:p.Pro1706Ala
|
|