ENST00000388913.4:c.967C>G
MANE Select
|
ENSP00000373565.3:p.Pro323Ala
|
|
ENST00000650760.1:c.1570C>G
|
ENSP00000499217.1:p.Pro524Ala
|
|
ENST00000388913.3:c.967C>G
|
ENSP00000373565.3:p.Pro323Ala
|
|
ENST00000395103.2:c.147C>G
|
|
|
NM_198488.3:c.967C>G
|
NP_940890.3:p.Pro323Ala
|
|
XM_005250887.2:c.1024C>G
|
XP_005250944.1:p.Pro342Ala
|
|
XM_005250888.2:c.985C>G
|
XP_005250945.1:p.Pro329Ala
|
|
XM_005250889.2:c.967C>G
|
XP_005250946.1:p.Pro323Ala
|
|
XM_011516980.1:c.1288C>G
|
XP_011515282.1:p.Pro430Ala
|
|
XM_011516981.1:c.1135C>G
|
XP_011515283.1:p.Pro379Ala
|
|
XM_005250887.3:c.1024C>G
|
XP_005250944.1:p.Pro342Ala
|
|
XM_005250888.3:c.985C>G
|
XP_005250945.1:p.Pro329Ala
|
|
XM_005250889.3:c.967C>G
|
XP_005250946.1:p.Pro323Ala
|
|
XM_011516980.2:c.1570C>G
|
XP_011515282.2:p.Pro524Ala
|
|
XM_011516981.2:c.1135C>G
|
XP_011515283.1:p.Pro379Ala
|
|
XM_024447131.1:c.967C>G
|
XP_024302899.1:p.Pro323Ala
|
|
NM_198488.4:c.967C>G
|
NP_940890.3:p.Pro323Ala
|
|
NM_198488.5:c.967C>G
MANE Select
|
NP_940890.4:p.Pro323Ala
|
|