ENST00000379644.9:c.1592T>G
MANE Select
|
ENSP00000368965.4:p.Ile531Ser
|
|
ENST00000379644.8:c.1592T>G
|
ENSP00000368965.4:p.Ile531Ser
|
|
ENST00000519705.1:n.908T>G
|
|
|
ENST00000521576.1:c.743T>G
|
ENSP00000429029.1:p.Ile248Ser
|
|
ENST00000523989.1:n.1905T>G
|
|
|
NM_152419.2:c.1592T>G
|
NP_689632.2:p.Ile531Ser
|
|
XM_005273409.1:c.1703T>G
|
XP_005273466.1:p.Ile568Ser
|
|
XM_005273410.1:c.1679T>G
|
XP_005273467.1:p.Ile560Ser
|
|
XM_005273411.1:c.1511T>G
|
XP_005273468.1:p.Ile504Ser
|
|
NM_001363227.1:c.1679T>G
|
NP_001350156.1:p.Ile560Ser
|
|
NM_001363228.1:c.1400T>G
|
NP_001350157.1:p.Ile467Ser
|
|
NM_001363229.1:c.728T>G
|
NP_001350158.1:p.Ile243Ser
|
|
NM_152419.3:c.1592T>G
MANE Select
|
NP_689632.2:p.Ile531Ser
|
|
NM_001363227.2:c.1679T>G
|
NP_001350156.1:p.Ile560Ser
|
|
NM_001363228.2:c.1400T>G
|
NP_001350157.1:p.Ile467Ser
|
|
NM_001363229.2:c.728T>G
|
NP_001350158.1:p.Ile243Ser
|
|