ENST00000388913.4:c.866C>G
MANE Select
|
ENSP00000373565.3:p.Ala289Gly
|
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ENST00000650760.1:c.1469C>G
|
ENSP00000499217.1:p.Ala490Gly
|
|
ENST00000388913.3:c.866C>G
|
ENSP00000373565.3:p.Ala289Gly
|
|
ENST00000395103.2:c.46C>G
|
|
|
NM_198488.3:c.866C>G
|
NP_940890.3:p.Ala289Gly
|
|
XM_005250887.2:c.923C>G
|
XP_005250944.1:p.Ala308Gly
|
|
XM_005250888.2:c.884C>G
|
XP_005250945.1:p.Ala295Gly
|
|
XM_005250889.2:c.866C>G
|
XP_005250946.1:p.Ala289Gly
|
|
XM_011516980.1:c.1187C>G
|
XP_011515282.1:p.Ala396Gly
|
|
XM_011516981.1:c.1034C>G
|
XP_011515283.1:p.Ala345Gly
|
|
XM_005250887.3:c.923C>G
|
XP_005250944.1:p.Ala308Gly
|
|
XM_005250888.3:c.884C>G
|
XP_005250945.1:p.Ala295Gly
|
|
XM_005250889.3:c.866C>G
|
XP_005250946.1:p.Ala289Gly
|
|
XM_011516980.2:c.1469C>G
|
XP_011515282.2:p.Ala490Gly
|
|
XM_011516981.2:c.1034C>G
|
XP_011515283.1:p.Ala345Gly
|
|
XM_024447131.1:c.866C>G
|
XP_024302899.1:p.Ala289Gly
|
|
NM_198488.4:c.866C>G
|
NP_940890.3:p.Ala289Gly
|
|
NM_198488.5:c.866C>G
MANE Select
|
NP_940890.4:p.Ala289Gly
|
|