ENST00000367651.4:c.776T>C
MANE Select
|
ENSP00000356623.2:p.Phe259Ser
|
|
ENST00000367651.3:c.776T>C
|
ENSP00000356623.2:p.Phe259Ser
|
|
ENST00000536159.2:c.776T>C
|
ENSP00000442831.1:p.Phe259Ser
|
|
ENST00000537332.2:c.791T>C
|
ENSP00000444198.2:p.Phe264Ser
|
|
ENST00000618718.1:c.605T>C
|
ENSP00000479918.1:p.Phe202Ser
|
|
NM_001168388.2:c.776T>C
|
NP_001161860.1:p.Phe259Ser
|
|
NM_001168389.2:c.791T>C
|
NP_001161861.2:p.Phe264Ser
|
|
NM_006079.4:c.776T>C
|
NP_006070.2:p.Phe259Ser
|
|
NM_006079.5:c.776T>C
MANE Select
|
NP_006070.2:p.Phe259Ser
|
|
NM_001168388.3:c.776T>C
|
NP_001161860.1:p.Phe259Ser
|
|
NM_001168389.3:c.791T>C
|
NP_001161861.2:p.Phe264Ser
|
|