ENST00000389048.8:c.3491T>A
MANE Select
|
ENSP00000373700.3:p.Phe1164Tyr
|
|
ENST00000431873.6:c.718T>A
|
|
|
ENST00000638605.1:n.368T>A
|
|
|
ENST00000642122.1:c.287T>A
|
ENSP00000493203.1:p.Phe96Tyr
|
|
ENST00000389048.7:c.3491T>A
|
ENSP00000373700.3:p.Phe1164Tyr
|
|
ENST00000431873.5:c.371T>A
|
ENSP00000414027.2:p.Phe124Tyr
|
|
ENST00000453137.1:c.185T>A
|
ENSP00000387488.1:p.Phe62Tyr
|
|
ENST00000618119.4:c.2360T>A
|
ENSP00000482733.1:p.Phe787Tyr
|
|
NM_004304.4:c.3491T>A
|
NP_004295.2:p.Phe1164Tyr
|
|
NM_001353765.1:c.287T>A
|
NP_001340694.1:p.Phe96Tyr
|
|
XM_024452778.1:c.644T>A
|
XP_024308546.1:p.Phe215Tyr
|
|
XM_024452779.1:c.287T>A
|
XP_024308547.1:p.Phe96Tyr
|
|
NM_004304.5:c.3491T>A
MANE Select
|
NP_004295.2:p.Phe1164Tyr
|
|
NM_001353765.2:c.287T>A
|
NP_001340694.1:p.Phe96Tyr
|
|