ENST00000356141.9:c.2186C>T
MANE Select
|
ENSP00000348460.4:p.Thr729Ile
|
|
ENST00000551634.6:c.2195C>T
|
ENSP00000448373.2:p.Thr732Ile
|
|
ENST00000680362.1:c.2086C>T
|
|
|
ENST00000681323.1:c.793+2912C>T
|
|
|
ENST00000346562.6:c.2090C>T
|
ENSP00000319610.5:p.Thr697Ile
|
|
ENST00000356141.8:c.2186C>T
|
ENSP00000348460.4:p.Thr729Ile
|
|
ENST00000357798.9:c.2147C>T
|
ENSP00000350446.5:p.Thr716Ile
|
|
ENST00000548645.5:c.2096C>T
|
ENSP00000448916.1:p.Thr699Ile
|
|
ENST00000551492.5:c.2201C>T
|
ENSP00000450392.1:p.Thr734Ile
|
|
ENST00000551634.5:c.2108C>T
|
ENSP00000448373.1:p.Thr703Ile
|
|
NM_001164749.1:c.2186C>T
|
NP_001158221.1:p.Thr729Ile
|
|
NM_001165893.1:c.2096C>T
|
NP_001159365.1:p.Thr699Ile
|
|
NM_022123.2:c.2090C>T
|
NP_071406.1:p.Thr697Ile
|
|
NM_173159.2:c.2147C>T
|
NP_775182.1:p.Thr716Ile
|
|
XM_005267991.2:c.2207C>T
|
XP_005268048.1:p.Thr736Ile
|
|
XM_005267992.2:c.2201C>T
|
XP_005268049.1:p.Thr734Ile
|
|
XM_005267993.2:c.2147C>T
|
XP_005268050.1:p.Thr716Ile
|
|
XM_011537067.1:c.2237C>T
|
XP_011535369.1:p.Thr746Ile
|
|
XM_011537068.1:c.2228C>T
|
XP_011535370.1:p.Thr743Ile
|
|
XM_011537069.1:c.2198C>T
|
XP_011535371.1:p.Thr733Ile
|
|
XM_011537070.1:c.2141C>T
|
XP_011535372.1:p.Thr714Ile
|
|
XM_011537071.1:c.2108C>T
|
XP_011535373.1:p.Thr703Ile
|
|
XM_011537072.1:c.2087C>T
|
XP_011535374.1:p.Thr696Ile
|
|
XM_011537073.1:c.1880C>T
|
XP_011535375.1:p.Thr627Ile
|
|
XM_011537074.1:c.1880C>T
|
XP_011535376.1:p.Thr627Ile
|
|
XM_005267991.3:c.2294C>T
|
XP_005268048.2:p.Thr765Ile
|
|
XM_005267992.3:c.2288C>T
|
XP_005268049.2:p.Thr763Ile
|
|
XM_011537067.2:c.2237C>T
|
XP_011535369.1:p.Thr746Ile
|
|
XM_011537069.2:c.2285C>T
|
XP_011535371.2:p.Thr762Ile
|
|
XM_011537070.2:c.2141C>T
|
XP_011535372.1:p.Thr714Ile
|
|
XM_011537071.2:c.2195C>T
|
XP_011535373.2:p.Thr732Ile
|
|
XM_011537072.2:c.2087C>T
|
XP_011535374.1:p.Thr696Ile
|
|
XM_017021582.1:c.2345C>T
|
XP_016877071.1:p.Thr782Ile
|
|
XM_017021583.1:c.2336C>T
|
XP_016877072.1:p.Thr779Ile
|
|
XM_017021584.1:c.2255C>T
|
XP_016877073.1:p.Thr752Ile
|
|
XM_017021585.1:c.2204C>T
|
XP_016877074.1:p.Thr735Ile
|
|
XM_017021586.1:c.1880C>T
|
XP_016877075.1:p.Thr627Ile
|
|
XM_017021587.1:c.1880C>T
|
XP_016877076.1:p.Thr627Ile
|
|
XM_017021588.1:c.1880C>T
|
XP_016877077.1:p.Thr627Ile
|
|
NM_001164749.2:c.2186C>T
MANE Select
|
NP_001158221.1:p.Thr729Ile
|
|
NM_001165893.2:c.2096C>T
|
NP_001159365.1:p.Thr699Ile
|
|
NM_022123.3:c.2090C>T
|
NP_071406.1:p.Thr697Ile
|
|
NM_173159.3:c.2147C>T
|
NP_775182.1:p.Thr716Ile
|
|
NM_001394988.1:c.2141C>T
|
NP_001381917.1:p.Thr714Ile
|
|
NM_001394989.1:c.2087C>T
|
NP_001381918.1:p.Thr696Ile
|
|