ENST00000256999.7:c.218T>C
MANE Select
|
ENSP00000256999.2:p.Phe73Ser
|
|
ENST00000256999.6:c.218T>C
|
ENSP00000256999.2:p.Phe73Ser
|
|
ENST00000340334.11:c.173T>C
|
ENSP00000344131.7:p.Phe58Ser
|
|
ENST00000343844.8:c.-333T>C
|
ENSP00000344086.4:n.-333T>C
|
|
ENST00000356696.7:c.218T>C
|
ENSP00000349129.3:p.Phe73Ser
|
|
ENST00000525826.5:c.218T>C
|
ENSP00000434928.1:p.Phe73Ser
|
|
ENST00000529117.1:c.47T>C
|
ENSP00000431577.1:p.Phe16Ser
|
|
ENST00000529646.5:n.233T>C
|
|
|
ENST00000529648.1:c.*209T>C
|
ENSP00000431263.1:n.*209T>C
|
|
ENST00000533034.1:c.173T>C
|
ENSP00000431463.1:p.Phe58Ser
|
|
ENST00000533510.5:c.*130T>C
|
ENSP00000436569.1:n.*130T>C
|
|
NM_001014986.1:c.218T>C
|
NP_001014986.1:p.Phe73Ser
|
|
NM_001193471.1:c.173T>C
|
NP_001180400.1:p.Phe58Ser
|
|
NM_001193472.1:c.173T>C
|
NP_001180401.1:p.Phe58Ser
|
|
NM_001193473.1:c.-333T>C
|
NP_001180402.1:n.-333T>C
|
|
NM_004476.1:c.218T>C
|
NP_004467.1:p.Phe73Ser
|
|
XM_011519958.1:c.173T>C
|
XP_011518260.1:p.Phe58Ser
|
|
NM_001014986.2:c.218T>C
|
NP_001014986.1:p.Phe73Ser
|
|
NM_001193471.2:c.173T>C
|
NP_001180400.1:p.Phe58Ser
|
|
NM_001193472.2:c.173T>C
|
NP_001180401.1:p.Phe58Ser
|
|
NM_001193473.2:c.-333T>C
|
NP_001180402.1:n.-333T>C
|
|
NM_001351236.1:c.47T>C
|
NP_001338165.1:p.Phe16Ser
|
|
NM_004476.2:c.218T>C
|
NP_004467.1:p.Phe73Ser
|
|
XM_011519958.3:c.383T>C
|
XP_011518260.2:p.Phe128Ser
|
|
XM_017017432.1:c.383T>C
|
XP_016872921.1:p.Phe128Ser
|
|
XM_017017433.2:c.383T>C
|
XP_016872922.1:p.Phe128Ser
|
|
XM_017017434.1:c.173T>C
|
XP_016872923.1:p.Phe58Ser
|
|
XM_017017435.2:c.173T>C
|
XP_016872924.1:p.Phe58Ser
|
|
XM_017017444.2:c.-520T>C
|
XP_016872933.1:n.-520T>C
|
|
XM_017017445.1:c.-520T>C
|
XP_016872934.1:n.-520T>C
|
|
XM_017017446.1:c.-520T>C
|
XP_016872935.1:n.-520T>C
|
|
XM_017017447.1:c.-520T>C
|
XP_016872936.1:n.-520T>C
|
|
XM_017017448.1:c.-520T>C
|
XP_016872937.1:n.-520T>C
|
|
XM_017017449.2:c.-520T>C
|
XP_016872938.1:n.-520T>C
|
|
XM_017017450.2:c.-520T>C
|
XP_016872939.1:n.-520T>C
|
|
XM_017017451.2:c.-520T>C
|
XP_016872940.1:n.-520T>C
|
|
XM_024448411.1:c.-3921T>C
|
XP_024304179.1:n.-3921T>C
|
|
XR_001747818.1:n.613T>C
|
|
|
XR_001747819.1:n.445T>C
|
|
|
NM_004476.3:c.218T>C
MANE Select
|
NP_004467.1:p.Phe73Ser
|
|
NM_001014986.3:c.218T>C
|
NP_001014986.1:p.Phe73Ser
|
|
NM_001193471.3:c.173T>C
|
NP_001180400.1:p.Phe58Ser
|
|
NM_001193472.3:c.173T>C
|
NP_001180401.1:p.Phe58Ser
|
|
NM_001193473.3:c.-333T>C
|
NP_001180402.1:n.-333T>C
|
|
NM_001351236.2:c.47T>C
|
NP_001338165.1:p.Phe16Ser
|
|