ENST00000224721.12:c.6365C>G
MANE Select
|
ENSP00000224721.9:p.Thr2122Ser
|
|
ENST00000224721.10:c.6380C>G
|
ENSP00000224721.8:p.Thr2127Ser
|
|
ENST00000622827.4:c.6365C>G
|
ENSP00000483211.1:p.Thr2122Ser
|
|
NM_022124.5:c.6365C>G
|
NP_071407.4:p.Thr2122Ser
|
|
XM_006717940.2:c.6560C>G
|
XP_006718003.1:p.Thr2187Ser
|
|
XM_006717942.2:c.6494C>G
|
XP_006718005.1:p.Thr2165Ser
|
|
XM_011540039.1:c.6557C>G
|
XP_011538341.1:p.Thr2186Ser
|
|
XM_011540040.1:c.6554C>G
|
XP_011538342.1:p.Thr2185Ser
|
|
XM_011540041.1:c.6500C>G
|
XP_011538343.1:p.Thr2167Ser
|
|
XM_011540042.1:c.6560C>G
|
XP_011538344.1:p.Thr2187Ser
|
|
XM_011540043.1:c.6560C>G
|
XP_011538345.1:p.Thr2187Ser
|
|
XM_011540044.1:c.6425C>G
|
XP_011538346.1:p.Thr2142Ser
|
|
XM_011540045.1:c.6560C>G
|
XP_011538347.1:p.Thr2187Ser
|
|
XM_011540046.1:c.6020C>G
|
XP_011538348.1:p.Thr2007Ser
|
|
XM_011540047.1:c.5378C>G
|
XP_011538349.1:p.Thr1793Ser
|
|
XM_011540048.1:c.6560C>G
|
XP_011538350.1:p.Thr2187Ser
|
|
XM_011540049.1:c.6560C>G
|
XP_011538351.1:p.Thr2187Ser
|
|
XM_011540050.1:c.6560C>G
|
XP_011538352.1:p.Thr2187Ser
|
|
XM_011540051.1:c.6560C>G
|
XP_011538353.1:p.Thr2187Ser
|
|
XM_011540052.1:c.2888C>G
|
XP_011538354.1:p.Thr963Ser
|
|
XR_945796.1:n.6803C>G
|
|
|
NM_022124.6:c.6365C>G
MANE Select
|
NP_071407.4:p.Thr2122Ser
|
|