|
ENST00000262457.7:c.1478T>C
MANE Select
|
ENSP00000262457.2:p.Leu493Ser
|
|
|
ENST00000262456.6:c.1478T>C
|
ENSP00000262456.2:p.Leu493Ser
|
|
|
ENST00000262457.6:c.1478T>C
|
ENSP00000262457.2:p.Leu493Ser
|
|
|
NM_014425.3:c.1478T>C
|
NP_055240.2:p.Leu493Ser
|
|
|
NM_183245.2:c.1478T>C
|
NP_899068.1:p.Leu493Ser
|
|
|
NR_051962.1:n.1787T>C
|
|
|
|
XM_005251923.3:c.1478T>C
|
XP_005251980.1:p.Leu493Ser
|
|
|
XM_005251924.3:c.1190T>C
|
XP_005251981.1:p.Leu397Ser
|
|
|
XM_011518531.1:c.1478T>C
|
XP_011516833.1:p.Leu493Ser
|
|
|
XM_011518532.1:c.1478T>C
|
XP_011516834.1:p.Leu493Ser
|
|
|
XM_011518533.1:c.1478T>C
|
XP_011516835.1:p.Leu493Ser
|
|
|
XM_011518534.1:c.1190T>C
|
XP_011516836.1:p.Leu397Ser
|
|
|
XM_011518535.1:c.1190T>C
|
XP_011516837.1:p.Leu397Ser
|
|
|
XM_011518536.1:c.1190T>C
|
XP_011516838.1:p.Leu397Ser
|
|
|
XM_011518537.1:c.1190T>C
|
XP_011516839.1:p.Leu397Ser
|
|
|
XM_011518538.1:c.1190T>C
|
XP_011516840.1:p.Leu397Ser
|
|
|
XM_011518539.1:c.1157T>C
|
XP_011516841.1:p.Leu386Ser
|
|
|
XM_011518540.1:c.1157T>C
|
XP_011516842.1:p.Leu386Ser
|
|
|
XM_011518541.1:c.1157T>C
|
XP_011516843.1:p.Leu386Ser
|
|
|
XM_011518542.1:c.1190T>C
|
XP_011516844.1:p.Leu397Ser
|
|
|
XM_011518543.1:c.500T>C
|
XP_011516845.1:p.Leu167Ser
|
|
|
XM_011518544.1:c.500T>C
|
XP_011516846.1:p.Leu167Ser
|
|
|
XR_242585.1:n.1734T>C
|
|
|
|
XR_242586.1:n.1734T>C
|
|
|
|
XR_428522.1:n.1734T>C
|
|
|
|
NM_001318381.1:c.1190T>C
|
NP_001305310.1:p.Leu397Ser
|
|
|
NM_001318382.1:c.500T>C
|
NP_001305311.1:p.Leu167Ser
|
|
|
NM_014425.4:c.1478T>C
|
NP_055240.2:p.Leu493Ser
|
|
|
NR_134606.1:n.1734T>C
|
|
|
|
NM_014425.5:c.1478T>C
MANE Select
|
NP_055240.2:p.Leu493Ser
|
|
|
NM_001318381.2:c.1190T>C
|
NP_001305310.1:p.Leu397Ser
|
|
|
NM_001318382.2:c.500T>C
|
NP_001305311.1:p.Leu167Ser
|
|
|
NR_134606.2:n.1676T>C
|
|
|
