|
ENST00000586569.3:c.421C>T
MANE Select
|
ENSP00000465500.1:p.His141Tyr
|
|
|
ENST00000639222.1:c.421C>T
|
ENSP00000492422.1:p.His141Tyr
|
|
|
ENST00000269485.11:c.421C>T
|
ENSP00000269485.7:p.His141Tyr
|
|
|
ENST00000586569.2:c.421C>T
|
ENSP00000465500.1:p.His141Tyr
|
|
|
ENST00000616710.4:c.421C>T
|
ENSP00000479567.1:p.His141Tyr
|
|
|
ENST00000617039.4:c.421C>T
|
ENSP00000482466.1:p.His141Tyr
|
|
|
NM_001270949.1:c.421C>T
|
NP_001257878.1:p.His141Tyr
|
|
|
NM_001270950.1:c.421C>T
|
NP_001257879.1:p.His141Tyr
|
|
|
NM_001270951.1:c.421C>T
|
NP_001257880.1:p.His141Tyr
|
|
|
NM_001278268.1:c.421C>T
|
NP_001265197.1:p.His141Tyr
|
|
|
NM_003839.3:c.421C>T
|
NP_003830.1:p.His141Tyr
|
|
|
XM_011526244.1:c.421C>T
|
XP_011524546.1:p.His141Tyr
|
|
|
XM_011526245.1:c.303C>T
|
XP_011524547.1:p.Ser101=
|
|
|
XR_935263.1:n.436C>T
|
|
|
|
XM_011526244.2:c.421C>T
|
XP_011524546.1:p.His141Tyr
|
|
|
XM_011526245.2:c.303C>T
|
XP_011524547.1:p.Ser101=
|
|
|
XM_017026064.1:c.303C>T
|
XP_016881553.1:p.Ser101=
|
|
|
XM_017026065.1:c.256C>T
|
XP_016881554.1:p.His86Tyr
|
|
|
XM_017026066.1:c.201C>T
|
XP_016881555.1:p.Ser67=
|
|
|
NM_003839.4:c.421C>T
MANE Select
|
NP_003830.1:p.His141Tyr
|
|
|
NM_001270951.2:c.421C>T
|
NP_001257880.1:p.His141Tyr
|
|
|
NM_001278268.2:c.421C>T
|
NP_001265197.1:p.His141Tyr
|
|
|
NM_001270949.2:c.421C>T
|
NP_001257878.1:p.His141Tyr
|
|
|
NM_001270950.2:c.421C>T
|
NP_001257879.1:p.His141Tyr
|
|
