NM_001361.5:c.1036C=
MANE Select
|
NP_001352.2:p.Arg346=
|
ENST00000219240.9:c.1036C=
MANE Select
|
ENSP00000219240.4:p.Arg346=
|
NM_001361.4:c.1036C=
|
NP_001352.2:p.Arg346=
|
ENST00000219240.8:c.1036C=
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ENSP00000219240.4:p.Arg346=
|
ENST00000571392.1:n.1700C=
|
|
ENST00000572887.5:c.1030C=
|
ENSP00000461848.1:p.Arg344=
|
ENST00000574309.5:c.514-609C=
|
|
XM_005255827.2:c.952C=
|
XP_005255884.1:p.Arg318=
|
XM_005255827.4:c.952C=
|
XP_005255884.1:p.Arg318=
|
XM_005255828.3:c.628C=
|
XP_005255885.1:p.Arg210=
|
XM_005255829.2:c.607C=
|
XP_005255886.1:p.Arg203=
|
XM_005255829.4:c.607C=
|
XP_005255886.1:p.Arg203=
|
XM_017022990.2:c.709C=
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XP_016878479.1:p.Arg237=
|