ENST00000703783.1:n.217G>T
|
|
|
ENST00000703785.1:n.298G>T
|
|
|
ENST00000262464.9:c.3433G>T
MANE Select
|
ENSP00000262464.4:p.Gly1145Cys
|
|
ENST00000262464.8:c.3433G>T
|
ENSP00000262464.4:p.Gly1145Cys
|
|
ENST00000507835.5:c.-18G>T
|
ENSP00000426839.1:n.-18G>T
|
|
ENST00000508053.5:c.3433G>T
|
ENSP00000424571.1:p.Gly1145Cys
|
|
ENST00000508989.5:c.3334G>T
|
ENSP00000425596.1:p.Gly1112Cys
|
|
ENST00000619499.4:c.3430G>T
|
ENSP00000482132.1:p.Gly1144Cys
|
|
NM_001999.3:c.3433G>T
|
NP_001990.2:p.Gly1145Cys
|
|
XM_017009228.2:c.3280G>T
|
XP_016864717.1:p.Gly1094Cys
|
|
NM_001999.4:c.3433G>T
MANE Select
|
NP_001990.2:p.Gly1145Cys
|
|