ENST00000301831.9:c.1607T>G
MANE Select
|
ENSP00000301831.4:p.Leu536Ter
|
|
ENST00000301831.8:c.1607T>G
|
ENSP00000301831.4:p.Leu536Ter
|
|
ENST00000420927.5:c.1607T>G
|
ENSP00000412187.1:p.Leu536Ter
|
|
NM_017886.2:c.1607T>G
|
NP_060356.2:p.Leu536Ter
|
|
XM_005265261.3:c.1604T>G
|
XP_005265318.1:p.Leu535Ter
|
|
XM_006713215.2:c.1250T>G
|
XP_006713278.1:p.Leu417Ter
|
|
XM_011533872.1:c.1607T>G
|
XP_011532174.1:p.Leu536Ter
|
|
XM_011533873.1:c.1607T>G
|
XP_011532175.1:p.Leu536Ter
|
|
XM_011533874.1:c.1607T>G
|
XP_011532176.1:p.Leu536Ter
|
|
XM_011533875.1:c.1607T>G
|
XP_011532177.1:p.Leu536Ter
|
|
XM_011533876.1:c.1607T>G
|
XP_011532178.1:p.Leu536Ter
|
|
XM_011533877.1:c.818T>G
|
XP_011532179.1:p.Leu273Ter
|
|
XM_011533878.1:c.1607T>G
|
XP_011532180.1:p.Leu536Ter
|
|
XM_011533879.1:c.467T>G
|
XP_011532181.1:p.Leu156Ter
|
|
XR_427279.2:n.2524T>G
|
|
|
NM_001322500.1:c.1607T>G
|
NP_001309429.1:p.Leu536Ter
|
|
NM_001322501.1:c.701T>G
|
NP_001309430.1:p.Leu234Ter
|
|
NM_017886.3:c.1607T>G
|
NP_060356.2:p.Leu536Ter
|
|
NR_136342.1:n.2010T>G
|
|
|
NM_017886.4:c.1607T>G
MANE Select
|
NP_060356.2:p.Leu536Ter
|
|
NM_001322500.2:c.1607T>G
|
NP_001309429.1:p.Leu536Ter
|
|
NM_001322501.2:c.701T>G
|
NP_001309430.1:p.Leu234Ter
|
|
NR_136342.2:n.1673T>G
|
|
|