ENST00000375708.4:c.182T>C
MANE Select
|
ENSP00000364860.3:p.Phe61Ser
|
|
ENST00000375708.3:c.182T>C
|
ENSP00000364860.3:p.Phe61Ser
|
|
ENST00000375715.5:c.-239T>C
|
ENSP00000364867.1:n.-239T>C
|
|
ENST00000495386.5:n.445T>C
|
|
|
ENST00000546883.1:n.384T>C
|
|
|
ENST00000548585.2:n.48T>C
|
|
|
ENST00000550066.5:n.650T>C
|
|
|
NM_004560.3:c.182T>C
|
NP_004551.2:p.Phe61Ser
|
|
XM_005252008.3:c.-239T>C
|
XP_005252065.1:n.-239T>C
|
|
XM_006717121.2:c.-239T>C
|
XP_006717184.1:n.-239T>C
|
|
XM_011518721.1:c.-239T>C
|
XP_011517023.1:n.-239T>C
|
|
NM_001318204.1:c.182T>C
|
NP_001305133.1:p.Phe61Ser
|
|
XM_005252008.4:c.-239T>C
|
XP_005252065.1:n.-239T>C
|
|
XM_006717121.3:c.-239T>C
|
XP_006717184.1:n.-239T>C
|
|
XM_017014762.1:c.173T>C
|
XP_016870251.1:p.Phe58Ser
|
|
XM_017014763.1:c.-239T>C
|
XP_016870252.1:n.-239T>C
|
|
XR_001746315.1:n.425T>C
|
|
|
NM_004560.4:c.182T>C
MANE Select
|
NP_004551.2:p.Phe61Ser
|
|
NM_001318204.2:c.182T>C
|
NP_001305133.1:p.Phe61Ser
|
|