ENST00000336411.7:c.1433T>C
|
ENSP00000337915.3:p.Phe478Ser
|
|
ENST00000651162.1:n.775T>C
|
|
|
ENST00000651514.1:c.1340T>C
MANE Select
|
ENSP00000498939.1:p.Phe447Ser
|
|
ENST00000651783.1:c.881T>C
|
ENSP00000498924.1:p.Phe294Ser
|
|
ENST00000652018.1:c.1193T>C
|
ENSP00000498733.1:p.Phe398Ser
|
|
ENST00000336411.6:c.1340T>C
|
ENSP00000337915.2:p.Phe447Ser
|
|
ENST00000354593.6:c.890T>C
|
ENSP00000346607.2:p.Phe297Ser
|
|
NM_001202855.2:c.1337T>C
|
NP_001189784.1:p.Phe446Ser
|
|
NM_017460.5:c.1340T>C
|
NP_059488.2:p.Phe447Ser
|
|
XM_011515841.1:c.1433T>C
|
XP_011514143.1:p.Phe478Ser
|
|
XM_011515842.1:c.1430T>C
|
XP_011514144.1:p.Phe477Ser
|
|
NM_017460.6:c.1340T>C
MANE Select
|
NP_059488.2:p.Phe447Ser
|
|
NM_001202855.3:c.1337T>C
|
NP_001189784.1:p.Phe446Ser
|
|