ENST00000470918.2:n.4534T>C
|
|
|
ENST00000695970.1:c.3332T>C
|
ENSP00000512297.1:p.Ile1111Thr
|
|
ENST00000695971.1:c.3485T>C
|
ENSP00000512298.1:p.Ile1162Thr
|
|
ENST00000695972.1:c.*583T>C
|
ENSP00000512299.1:n.*583T>C
|
|
ENST00000695973.1:c.*1870T>C
|
ENSP00000512300.1:n.*1870T>C
|
|
ENST00000695974.1:c.3329T>C
|
ENSP00000512301.1:p.Ile1110Thr
|
|
ENST00000695975.1:c.*1633T>C
|
ENSP00000512302.1:n.*1633T>C
|
|
ENST00000695976.1:c.3317T>C
|
ENSP00000512303.1:p.Ile1106Thr
|
|
ENST00000695981.1:c.3506T>C
|
ENSP00000512306.1:p.Ile1169Thr
|
|
ENST00000695984.1:c.1514T>C
|
ENSP00000512309.1:p.Ile505Thr
|
|
ENST00000695986.1:c.*3157T>C
|
ENSP00000512311.1:n.*3157T>C
|
|
ENST00000695990.1:n.540T>C
|
|
|
ENST00000696026.1:c.*1788T>C
|
ENSP00000512335.1:n.*1788T>C
|
|
ENST00000696027.1:c.3500T>C
|
ENSP00000512336.1:p.Ile1167Thr
|
|
ENST00000696028.1:c.3434T>C
|
ENSP00000512337.1:p.Ile1145Thr
|
|
ENST00000696029.1:c.3500T>C
|
ENSP00000512338.1:p.Ile1167Thr
|
|
ENST00000696031.1:c.*3024T>C
|
ENSP00000512340.1:n.*3024T>C
|
|
ENST00000696032.1:c.3506T>C
|
ENSP00000512341.1:p.Ile1169Thr
|
|
ENST00000696033.1:c.1160-32674T>C
|
ENSP00000512342.1:n.1160-32674T>C
|
|
ENST00000367429.9:c.3506T>C
MANE Select
|
ENSP00000356399.4:p.Ile1169Thr
|
|
ENST00000367429.8:c.3506T>C
|
ENSP00000356399.4:p.Ile1169Thr
|
|
ENST00000466229.5:n.6604T>C
|
|
|
NM_000186.3:c.3506T>C , LRG_47t1:c.3506T>C
|
NP_000177.2:p.Ile1169Thr
|
|
XR_001737134.2:n.3692T>C
|
|
|
NM_000186.4:c.3506T>C
MANE Select
|
NP_000177.2:p.Ile1169Thr
|
|