ENST00000305242.10:c.2617G>A
MANE Select
|
ENSP00000306410.5:p.Gly873Arg
|
|
ENST00000672841.1:c.1693G>A
|
ENSP00000499983.1:p.Gly565Arg
|
|
ENST00000672877.1:c.1192G>A
|
ENSP00000500120.1:p.Gly398Arg
|
|
ENST00000673384.1:c.1693G>A
|
ENSP00000500856.1:p.Gly565Arg
|
|
ENST00000673439.1:c.2617G>A
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ENSP00000500782.1:p.Gly873Arg
|
|
ENST00000305242.9:c.2617G>A
|
ENSP00000306410.5:p.Gly873Arg
|
|
NM_001290020.1:c.2617G>A
|
NP_001276949.1:p.Gly873Arg
|
|
NM_001290021.1:c.1192G>A
|
NP_001276950.1:p.Gly398Arg
|
|
NM_001312689.1:c.1693G>A
|
NP_001299618.1:p.Gly565Arg
|
|
NM_018076.3:c.2617G>A
|
NP_060546.2:p.Gly873Arg
|
|
NM_018076.4:c.2617G>A
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NP_060546.2:p.Gly873Arg
|
|
XM_011519526.1:c.2617G>A
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XP_011517828.1:p.Gly873Arg
|
|
XM_011519527.1:c.2617G>A
|
XP_011517829.1:p.Gly873Arg
|
|
XM_011519528.1:c.2617G>A
|
XP_011517830.1:p.Gly873Arg
|
|
XM_011519529.1:c.2617G>A
|
XP_011517831.1:p.Gly873Arg
|
|
XM_011519530.1:c.2617G>A
|
XP_011517832.1:p.Gly873Arg
|
|
XM_011519531.1:c.2617G>A
|
XP_011517833.1:p.Gly873Arg
|
|
XM_011519532.1:c.2407G>A
|
XP_011517834.1:p.Gly803Arg
|
|
XM_011519533.1:c.1693G>A
|
XP_011517835.1:p.Gly565Arg
|
|
XM_011519534.1:c.1693G>A
|
XP_011517836.1:p.Gly565Arg
|
|
XM_011519535.1:c.1531G>A
|
XP_011517837.1:p.Gly511Arg
|
|
XM_011519537.1:c.1192G>A
|
XP_011517839.1:p.Gly398Arg
|
|
XM_024448049.1:c.2746G>A
|
XP_024303817.1:p.Gly916Arg
|
|
XM_024448050.1:c.2746G>A
|
XP_024303818.1:p.Gly916Arg
|
|
XM_024448051.1:c.2746G>A
|
XP_024303819.1:p.Gly916Arg
|
|
XM_024448052.1:c.2746G>A
|
XP_024303820.1:p.Gly916Arg
|
|
XM_024448053.1:c.2746G>A
|
XP_024303821.1:p.Gly916Arg
|
|
XM_024448054.1:c.2536G>A
|
XP_024303822.1:p.Gly846Arg
|
|
XM_024448055.1:c.1822G>A
|
XP_024303823.1:p.Gly608Arg
|
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XM_024448056.1:c.1822G>A
|
XP_024303824.1:p.Gly608Arg
|
|
XM_024448057.1:c.1660G>A
|
XP_024303825.1:p.Gly554Arg
|
|
XM_024448058.1:c.1321G>A
|
XP_024303826.1:p.Gly441Arg
|
|
NM_001290020.2:c.2617G>A
|
NP_001276949.1:p.Gly873Arg
|
|
NM_001290021.2:c.1192G>A
|
NP_001276950.1:p.Gly398Arg
|
|
NM_001312689.2:c.1693G>A
|
NP_001299618.1:p.Gly565Arg
|
|
NM_018076.5:c.2617G>A
MANE Select
|
NP_060546.2:p.Gly873Arg
|
|