ENST00000376199.7:c.887T>C
|
ENSP00000365372.2:p.Phe296Ser
|
|
ENST00000376207.10:c.992T>C
MANE Select
|
ENSP00000365380.4:p.Phe331Ser
|
|
ENST00000455775.7:c.1061T>C
|
ENSP00000396415.3:p.Phe354Ser
|
|
ENST00000518685.6:c.911T>C
|
ENSP00000428952.2:p.Phe304Ser
|
|
ENST00000557224.6:c.887T>C
|
ENSP00000451208.1:p.Phe296Ser
|
|
ENST00000651307.1:c.967+739T>C
|
ENSP00000498454.1:n.967+739T>C
|
|
ENST00000376197.1:c.842T>C
|
ENSP00000365369.1:p.Phe281Ser
|
|
ENST00000376199.6:c.887T>C
|
ENSP00000365372.2:p.Phe296Ser
|
|
ENST00000376207.8:c.992T>C
|
ENSP00000365380.4:p.Phe331Ser
|
|
ENST00000455775.6:c.1061T>C
|
ENSP00000396415.3:p.Phe354Ser
|
|
ENST00000518685.5:c.887T>C
|
ENSP00000428952.1:p.Phe296Ser
|
|
ENST00000557224.5:c.887T>C
|
ENSP00000451208.1:p.Phe296Ser
|
|
NM_001114377.1:c.887T>C
|
NP_001107849.1:p.Phe296Ser
|
|
NM_014009.3:c.992T>C , LRG_62t1:c.992T>C
|
NP_054728.2:p.Phe331Ser
|
|
XM_006724533.2:c.1061T>C
|
XP_006724596.2:p.Phe354Ser
|
|
XM_011543915.1:c.1211T>C
|
XP_011542217.1:p.Phe404Ser
|
|
XM_011543916.1:c.1211T>C
|
XP_011542218.1:p.Phe404Ser
|
|
XM_011543917.1:c.1010T>C
|
XP_011542219.1:p.Phe337Ser
|
|
XM_011543918.1:c.1247T>C
|
XP_011542220.1:p.Phe416Ser
|
|
XM_011543919.1:c.1211T>C
|
XP_011542221.1:p.Phe404Ser
|
|
XM_017029567.1:c.938T>C
|
XP_016885056.1:p.Phe313Ser
|
|
NM_001114377.2:c.887T>C
|
NP_001107849.1:p.Phe296Ser
|
|
NM_014009.4:c.992T>C
MANE Select
|
NP_054728.2:p.Phe331Ser
|
|