ENST00000388913.4:c.1177G>T
MANE Select
|
ENSP00000373565.3:p.Ala393Ser
|
|
ENST00000650760.1:c.1780G>T
|
ENSP00000499217.1:p.Ala594Ser
|
|
ENST00000388913.3:c.1177G>T
|
ENSP00000373565.3:p.Ala393Ser
|
|
ENST00000395103.2:c.357G>T
|
|
|
NM_198488.3:c.1177G>T
|
NP_940890.3:p.Ala393Ser
|
|
XM_005250887.2:c.1234G>T
|
XP_005250944.1:p.Ala412Ser
|
|
XM_005250888.2:c.1195G>T
|
XP_005250945.1:p.Ala399Ser
|
|
XM_005250889.2:c.1177G>T
|
XP_005250946.1:p.Ala393Ser
|
|
XM_011516980.1:c.1498G>T
|
XP_011515282.1:p.Ala500Ser
|
|
XM_011516981.1:c.1345G>T
|
XP_011515283.1:p.Ala449Ser
|
|
XM_005250887.3:c.1234G>T
|
XP_005250944.1:p.Ala412Ser
|
|
XM_005250888.3:c.1195G>T
|
XP_005250945.1:p.Ala399Ser
|
|
XM_005250889.3:c.1177G>T
|
XP_005250946.1:p.Ala393Ser
|
|
XM_011516980.2:c.1780G>T
|
XP_011515282.2:p.Ala594Ser
|
|
XM_011516981.2:c.1345G>T
|
XP_011515283.1:p.Ala449Ser
|
|
XM_024447131.1:c.1177G>T
|
XP_024302899.1:p.Ala393Ser
|
|
NM_198488.4:c.1177G>T
|
NP_940890.3:p.Ala393Ser
|
|
NM_198488.5:c.1177G>T
MANE Select
|
NP_940890.4:p.Ala393Ser
|
|