ENST00000281928.9:c.3110T>G
MANE Select
|
ENSP00000281928.3:p.Val1037Gly
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|
ENST00000548743.2:c.3080T>G
|
ENSP00000448553.2:p.Val1027Gly
|
|
ENST00000549786.2:c.2538T>G
|
|
|
ENST00000648173.1:n.1905T>G
|
|
|
ENST00000648379.1:n.1478T>G
|
|
|
ENST00000648737.1:n.2874T>G
|
|
|
ENST00000648916.1:n.1121T>G
|
|
|
ENST00000649607.1:c.1294T>G
|
|
|
ENST00000650226.1:c.3110T>G
|
ENSP00000496981.1:p.Val1037Gly
|
|
ENST00000281928.7:c.3110T>G
|
ENSP00000281928.3:p.Val1037Gly
|
|
NM_015335.4:c.3110T>G
|
NP_056150.1:p.Val1037Gly
|
|
XM_011538080.1:c.3110T>G
|
XP_011536382.1:p.Val1037Gly
|
|
XM_011538081.1:c.3107T>G
|
XP_011536383.1:p.Val1036Gly
|
|
XM_011538082.1:c.3080T>G
|
XP_011536384.1:p.Val1027Gly
|
|
XM_011538080.2:c.3110T>G
|
XP_011536382.1:p.Val1037Gly
|
|
XM_011538081.2:c.3107T>G
|
XP_011536383.1:p.Val1036Gly
|
|
XM_011538082.2:c.3080T>G
|
XP_011536384.1:p.Val1027Gly
|
|
XM_017019090.1:c.3107T>G
|
XP_016874579.1:p.Val1036Gly
|
|
NM_015335.5:c.3110T>G
MANE Select
|
NP_056150.1:p.Val1037Gly
|
|