ENST00000704074.1:c.312+52C>G
|
|
|
ENST00000283179.14:c.634+52C>G
|
ENSP00000283179.10:n.634+52C>G
|
|
ENST00000444376.7:c.634+52C>G
|
ENSP00000393151.2:n.634+52C>G
|
|
ENST00000476241.2:n.819+52C>G
|
|
|
ENST00000638475.1:c.418+52C>G
|
ENSP00000491305.1:n.418+52C>G
|
|
ENST00000638952.1:n.917C>G
|
|
|
ENST00000640056.1:c.32C>G
|
ENSP00000492620.1:p.Ala11Gly
|
|
ENST00000640218.2:c.686C>G
MANE Select
|
ENSP00000491215.1:p.Ala229Gly
|
|
ENST00000640306.1:c.634+52C>G
|
ENSP00000491685.1:n.634+52C>G
|
|
ENST00000640440.1:c.334+52C>G
|
ENSP00000491263.1:n.334+52C>G
|
|
ENST00000649899.1:n.858+52C>G
|
|
|
ENST00000283179.13:c.686C>G
|
ENSP00000283179.9:p.Ala229Gly
|
|
ENST00000444376.6:c.634+52C>G
|
ENSP00000393151.2:n.634+52C>G
|
|
ENST00000476241.1:n.818+52C>G
|
|
|
NM_004501.3:c.634+52C>G
|
NP_004492.2:n.634+52C>G
|
|
NM_031844.2:c.686C>G
|
NP_114032.2:p.Ala229Gly
|
|
NM_031844.3:c.686C>G
MANE Select
|
NP_114032.2:p.Ala229Gly
|
|