ENST00000388913.4:c.812A>C
MANE Select
|
ENSP00000373565.3:p.Asp271Ala
|
|
ENST00000650760.1:c.1415A>C
|
ENSP00000499217.1:p.Asp472Ala
|
|
ENST00000388913.3:c.812A>C
|
ENSP00000373565.3:p.Asp271Ala
|
|
NM_198488.3:c.812A>C
|
NP_940890.3:p.Asp271Ala
|
|
XM_005250887.2:c.869A>C
|
XP_005250944.1:p.Asp290Ala
|
|
XM_005250888.2:c.830A>C
|
XP_005250945.1:p.Asp277Ala
|
|
XM_005250889.2:c.812A>C
|
XP_005250946.1:p.Asp271Ala
|
|
XM_011516980.1:c.1133A>C
|
XP_011515282.1:p.Asp378Ala
|
|
XM_011516981.1:c.980A>C
|
XP_011515283.1:p.Asp327Ala
|
|
XM_005250887.3:c.869A>C
|
XP_005250944.1:p.Asp290Ala
|
|
XM_005250888.3:c.830A>C
|
XP_005250945.1:p.Asp277Ala
|
|
XM_005250889.3:c.812A>C
|
XP_005250946.1:p.Asp271Ala
|
|
XM_011516980.2:c.1415A>C
|
XP_011515282.2:p.Asp472Ala
|
|
XM_011516981.2:c.980A>C
|
XP_011515283.1:p.Asp327Ala
|
|
XM_024447131.1:c.812A>C
|
XP_024302899.1:p.Asp271Ala
|
|
NM_198488.4:c.812A>C
|
NP_940890.3:p.Asp271Ala
|
|
NM_198488.5:c.812A>C
MANE Select
|
NP_940890.4:p.Asp271Ala
|
|