ENST00000053867.8:c.1408C>G
MANE Select
|
ENSP00000053867.2:p.Pro470Ala
|
|
ENST00000639447.1:c.1137-286C>G
|
ENSP00000492014.1:n.1137-286C>G
|
|
ENST00000053867.7:c.1408C>G
|
ENSP00000053867.2:p.Pro470Ala
|
|
ENST00000586242.1:c.42C>G
|
|
|
ENST00000586443.1:c.849C>G
|
|
|
ENST00000589265.5:c.937C>G
|
ENSP00000467616.1:p.Pro313Ala
|
|
NM_002087.3:c.1408C>G
|
NP_002078.1:p.Pro470Ala
|
|
XM_005257253.1:c.1408C>G
|
XP_005257310.1:p.Pro470Ala
|
|
XM_024450730.1:c.1408C>G
|
XP_024306498.1:p.Pro470Ala
|
|
NM_002087.4:c.1408C>G
MANE Select
|
NP_002078.1:p.Pro470Ala
|
|