ENST00000372470.9:c.278G>A
MANE Select
|
ENSP00000361548.3:p.Cys93Tyr
|
|
ENST00000413998.7:c.257G>A
|
ENSP00000414004.3:p.Cys86Tyr
|
|
ENST00000638732.1:n.278G>A
|
|
|
ENST00000372470.7:c.278G>A
|
ENSP00000361548.3:p.Cys93Tyr
|
|
ENST00000413998.6:c.278G>A
|
ENSP00000414004.2:p.Cys93Tyr
|
|
ENST00000612993.1:c.278G>A
|
ENSP00000480273.1:p.Cys93Tyr
|
|
NM_005373.2:c.278G>A , LRG_510t1:c.278G>A
|
NP_005364.1:p.Cys93Tyr
|
|
XM_011541478.1:c.257G>A
|
XP_011539780.1:p.Cys86Tyr
|
|
XM_017001320.1:c.449G>A
|
XP_016856809.1:p.Cys150Tyr
|
|
NM_005373.3:c.278G>A
MANE Select
|
NP_005364.1:p.Cys93Tyr
|
|