ENST00000299506.3:c.182C>G
MANE Select
|
ENSP00000299506.3:p.Ala61Gly
|
|
ENST00000299506.2:c.182C>G
|
ENSP00000299506.2:p.Ala61Gly
|
|
ENST00000305253.8:c.347C>G
|
ENSP00000305426.4:p.Ala116Gly
|
|
ENST00000534099.5:c.200C>G
|
ENSP00000434400.1:p.Ala67Gly
|
|
NM_003320.4:c.347C>G
|
NP_003311.2:p.Ala116Gly
|
|
NM_177972.2:c.182C>G
|
NP_813977.1:p.Ala61Gly
|
|
XM_005253109.2:c.308C>G
|
XP_005253166.1:p.Ala103Gly
|
|
XM_011520344.1:c.218C>G
|
XP_011518646.1:p.Ala73Gly
|
|
XM_005253109.3:c.308C>G
|
XP_005253166.1:p.Ala103Gly
|
|
XM_011520344.2:c.218C>G
|
XP_011518646.1:p.Ala73Gly
|
|
NM_177972.3:c.182C>G
MANE Select
|
NP_813977.1:p.Ala61Gly
|
|
NM_003320.5:c.347C>G
|
NP_003311.2:p.Ala116Gly
|
|