ENST00000389048.8:c.3578T>C
MANE Select
|
ENSP00000373700.3:p.Phe1193Ser
|
|
ENST00000431873.6:c.805T>C
|
|
|
ENST00000638605.1:n.455T>C
|
|
|
ENST00000642122.1:c.374T>C
|
ENSP00000493203.1:p.Phe125Ser
|
|
ENST00000389048.7:c.3578T>C
|
ENSP00000373700.3:p.Phe1193Ser
|
|
ENST00000431873.5:c.458T>C
|
ENSP00000414027.2:p.Phe153Ser
|
|
ENST00000618119.4:c.2447T>C
|
ENSP00000482733.1:p.Phe816Ser
|
|
NM_004304.4:c.3578T>C
|
NP_004295.2:p.Phe1193Ser
|
|
NM_001353765.1:c.374T>C
|
NP_001340694.1:p.Phe125Ser
|
|
XM_024452778.1:c.731T>C
|
XP_024308546.1:p.Phe244Ser
|
|
XM_024452779.1:c.374T>C
|
XP_024308547.1:p.Phe125Ser
|
|
NM_004304.5:c.3578T>C
MANE Select
|
NP_004295.2:p.Phe1193Ser
|
|
NM_001353765.2:c.374T>C
|
NP_001340694.1:p.Phe125Ser
|
|