ENST00000338037.11:c.2084C>T
MANE Select
|
ENSP00000338185.6:p.Thr695Ile
|
|
ENST00000635830.1:n.2155C>T
|
|
|
ENST00000636825.1:n.1948C>T
|
|
|
ENST00000637919.1:c.1781C>T
|
ENSP00000490862.1:p.Thr594Ile
|
|
ENST00000338037.10:c.2084C>T
|
ENSP00000338185.6:p.Thr695Ile
|
|
ENST00000378637.6:c.2084C>T
|
ENSP00000367904.2:p.Thr695Ile
|
|
ENST00000378641.7:c.2084C>T
|
ENSP00000367908.3:p.Thr695Ile
|
|
ENST00000439627.2:c.41C>T
|
ENSP00000391162.1:p.Thr14Ile
|
|
ENST00000487210.5:c.1306C>T
|
|
|
ENST00000494924.2:n.1236C>T
|
|
|
ENST00000612075.4:c.1844C>T
|
ENSP00000479997.1:p.Thr615Ile
|
|
ENST00000617005.4:c.1844C>T
|
ENSP00000477664.1:p.Thr615Ile
|
|
ENST00000625874.2:c.1781C>T
|
ENSP00000486301.1:p.Thr594Ile
|
|
ENST00000626966.2:c.1781C>T
|
ENSP00000487075.1:p.Thr594Ile
|
|
NM_015192.3:c.2084C>T
|
NP_056007.1:p.Thr695Ile
|
|
NM_182734.2:c.2084C>T
|
NP_877398.1:p.Thr695Ile
|
|
XM_011529199.1:c.2084C>T
|
XP_011527501.1:p.Thr695Ile
|
|
XM_011529200.1:c.1868C>T
|
XP_011527502.1:p.Thr623Ile
|
|
XM_011529201.1:c.1781C>T
|
XP_011527503.1:p.Thr594Ile
|
|
XM_011529203.1:c.311C>T
|
XP_011527505.1:p.Thr104Ile
|
|
NM_015192.4:c.2084C>T
MANE Select
|
NP_056007.1:p.Thr695Ile
|
|
NM_182734.3:c.2084C>T
|
NP_877398.1:p.Thr695Ile
|
|