ENST00000322776.11:c.684C>G
MANE Select
|
ENSP00000322450.6:p.Pro228=
|
|
ENST00000647561.1:c.684C>G
|
ENSP00000497587.1:p.Pro228=
|
|
ENST00000322776.10:c.684C>G
|
ENSP00000322450.6:p.Pro228=
|
|
ENST00000415352.6:c.663C>G
|
ENSP00000395368.2:p.Pro221=
|
|
ENST00000526169.1:n.426C>G
|
|
|
ENST00000526770.5:n.543C>G
|
|
|
ENST00000529927.5:c.657C>G
|
ENSP00000436766.1:p.Pro219=
|
|
ENST00000532244.5:c.381C>G
|
ENSP00000435202.1:p.Pro127=
|
|
ENST00000532303.5:c.381C>G
|
ENSP00000432015.1:p.Pro127=
|
|
ENST00000533919.5:c.162C>G
|
ENSP00000435199.1:p.Pro54=
|
|
NM_001166102.1:c.657C>G
|
NP_001159574.1:p.Pro219=
|
|
NM_007103.3:c.684C>G
|
NP_009034.2:p.Pro228=
|
|
NM_001166102.2:c.657C>G
|
NP_001159574.1:p.Pro219=
|
|
NM_007103.4:c.684C>G
MANE Select
|
NP_009034.2:p.Pro228=
|
|