ENST00000641284.2:c.*50C>G
|
ENSP00000493088.1:n.*50C>G
|
|
ENST00000646677.2:c.*701C>G
|
ENSP00000496533.1:n.*701C>G
|
|
ENST00000697428.1:n.2414C>G
|
|
|
ENST00000641284.1:c.*50C>G
|
ENSP00000493088.1:n.*50C>G
|
|
ENST00000646677.1:c.*701C>G
|
ENSP00000496533.1:n.*701C>G
|
|
ENST00000647318.2:c.2936C>G
MANE Select
|
ENSP00000495993.1:p.Ala979Gly
|
|
ENST00000300589.6:c.3017C>G
|
ENSP00000300589.2:p.Ala1006Gly
|
|
NM_001293557.1:c.2936C>G
|
NP_001280486.1:p.Ala979Gly
|
|
NM_022162.2:c.3017C>G
|
NP_071445.1:p.Ala1006Gly
|
|
XM_005256084.2:c.2936C>G
|
XP_005256141.1:p.Ala979Gly
|
|
XM_006721242.2:c.2852C>G
|
XP_006721305.1:p.Ala951Gly
|
|
XM_011523257.1:c.2513C>G
|
XP_011521559.1:p.Ala838Gly
|
|
XM_011523258.1:c.2513C>G
|
XP_011521560.1:p.Ala838Gly
|
|
XM_011523259.1:c.2351C>G
|
XP_011521561.1:p.Ala784Gly
|
|
XM_005256084.4:c.2936C>G
|
XP_005256141.1:p.Ala979Gly
|
|
XM_006721242.4:c.2852C>G
|
XP_006721305.1:p.Ala951Gly
|
|
XM_011523259.2:c.2351C>G
|
XP_011521561.1:p.Ala784Gly
|
|
XM_017023535.1:c.2444C>G
|
XP_016879024.1:p.Ala815Gly
|
|
XM_017023536.1:c.2351C>G
|
XP_016879025.1:p.Ala784Gly
|
|
XM_017023537.1:c.2351C>G
|
XP_016879026.1:p.Ala784Gly
|
|
XM_017023538.1:c.2351C>G
|
XP_016879027.1:p.Ala784Gly
|
|
NM_001293557.2:c.2936C>G
|
NP_001280486.1:p.Ala979Gly
|
|
NM_001370466.1:c.2936C>G
MANE Select
|
NP_001357395.1:p.Ala979Gly
|
|
NM_022162.3:c.3017C>G
|
NP_071445.1:p.Ala1006Gly
|
|
NR_163434.1:n.3148C>G
|
|
|